Showing 1–500 of 700 results
Acarbose Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets. The dosing is highly dependent on patient tolerance to GI side effects.
Active Ingredient Strength (Standard) Role Acarbose USP/BP 25 mg Initiation Dose (To minimize gas) Acarbose USP/BP 50 mg Standard Maintenance Dose Acarbose USP/BP 100 mg High Carbohydrate Load Dose Excipients Q.S. Microcrystalline Cellulose / Magnesium Stearate Aceclofenac & Thiocolchicoside Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the semi-synthetic Thiocolchicoside component.
Active Ingredient Strength Primary Clinical Use Aceclofenac BP/Ph.Eur.
Thiocolchicoside INN/Ph.Eur.100 mg
4 mgStandard Orthopedic Dose: Twice-daily therapy for moderate-to-severe acute back pain and torticollis. Aceclofenac BP/Ph.Eur.
Thiocolchicoside INN/Ph.Eur.100 mg
8 mgSevere Trauma Dose: Maximum therapy for severe, immobilizing orthopedic spasms (strictly twice daily). Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate Diluent / Superdisintegrant (Engineered for immediate gastric dissolution and rapid onset of relief) Aceclofenac Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. We utilize advanced solubilizing agents to ensure the drug remains stable in liquid form.
Active Ingredient Strength (Standard) Therapeutic Role Aceclofenac BP/IP 150 mg / ml Analgesic / Anti-inflammatory Excipients Q.S. Benzyl Alcohol / Propylene Glycol Preservative / Co-solvent *Pack Sizes: Tray of 5 Ampoules (1ml each) or 10 Ampoules.
Aceclofenac Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Standard) or Sustained Release (SR) Tablets.
Active Ingredient Strength Release Type Role Aceclofenac IP/BP/USP 100 mg Immediate Release Standard Adult Dose Aceclofenac IP/BP/USP 200 mg Sustained Release (SR) Once Daily Dosing Excipients Q.S. — Disintegrant / Binder Acetazolamide Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White, round). The 250 mg strength is the universal standard.
Active Ingredient Strength (Standard) Primary Role Acetazolamide USP/BP/IP 250 mg Glaucoma / Altitude Sickness / Edema Excipients Q.S. Starch / Povidone / Sodium Starch Glycolate Acyclovir Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated, Dispersible Tablets (often flavored/sweetened for palatability), packed in moisture-resistant blister strips.
Active Ingredient Strength Primary Clinical Use Acyclovir USP/BP/Ph.Eur. 200 mg HSV-1 & HSV-2 (Genital/Labial Herpes) Treatment Acyclovir USP/BP/Ph.Eur. 400 mg Recurrent HSV Suppression / Chronic Prophylaxis Acyclovir USP/BP/Ph.Eur. 800 mg Varicella (Chickenpox) & Herpes Zoster (Shingles) Excipients Crospovidone / Aspartame / Flavoring Agents Superdisintegrant / Sweetener / Taste-Masking Acyclovir injection
Freecomposition
Aciclovir 400 mg
Each Uncoated contains:
Aciclovir IP 400 mg
Excipients – QSAciclovir 200 mg
Each Uncoated Contains :
Aciclovir 200 mg
Excipients q.sUsage :- Treat infections caused by certain types of viruses
Category :- Antibiotic drugs
Therapeutic category :- Antiviral
Pcd pharma franchise :-
Pcd marketing :-
Manufacturer :- Healthy Life Pharma Pvt Ltd
Exporter :- Healthy Inc
Supplier :- Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor :- Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller :- Healthy Life Pharma Pvt Ltd
Healthy Inc
Acyclovir Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Dispersible Tablets (DT). The dosage varies significantly based on the viral strain being treated.
Active Ingredient Strength (Standard) Primary Indication Acyclovir USP/BP/IP 200 mg Herpes Simplex (Genital/Labial) Acyclovir USP/BP/IP 400 mg Suppression / Prophylaxis Acyclovir USP/BP/IP 800 mg Shingles (Herpes Zoster) / Chickenpox Excipients Q.S. Disintegrant / Binder Adrenaline Injections
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. The formulation includes stabilizers to prevent rapid oxidation.
Active Ingredient Strength (Standard 1:1000) Therapeutic Role Adrenaline Bitartrate BP/USP Eq. to Adrenaline 1 mg / ml Vasopressor / Bronchodilator Excipients Q.S. Sodium Metabisulfite / Sodium Chloride Antioxidant / Isotonicity *Pack Sizes: Tray of 10 Ampoules (1ml each) or Box of 50/100 Ampoules (Hospital Pack).
Adrenochrome Monosemicarbazone Tablet
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (often Orange/Red) to protect the drug from oxidation and light.
Active Ingredient Strength (Standard) Formulation Type Primary Role Adrenochrome Monosemicarbazone 10 mg Sugar Coated Tablet Minor Bleeding / Maintenance Adrenochrome Monosemicarbazone 25 mg / 30 mg Sugar Coated Tablet Surgical Prophylaxis Excipients Q.S. Titanium Dioxide / Sucrose Light Protection Coating Albendazole Tablet
Freeduct Composition & Strength
We supply this product as Chewable Tablets (Fruit Flavored) or Standard Film Coated Tablets. The chewable format is critical for Mass Drug Administration (MDA) in children.
Active Ingredient Strength (Standard) Formulation Type Role Albendazole USP/BP 200 mg Chewable / Film Coated Pediatric (1-2 Years) Albendazole USP/BP 400 mg Chewable (Uncoated) Standard Adult / MDA Dose Albendazole USP/BP 400 mg Film Coated Systemic Therapy Excipients Q.S. Mannitol / Orange Flavor Palatability Alendronate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Oval). The 70 mg strength is the international standard for weekly administration.
Active Ingredient Strength (Standard) Dosing Frequency Role Alendronate Sodium USP/BP 10 mg Once Daily Maintenance / Male Osteoporosis Alendronate Sodium USP/BP 70 mg Once Weekly Postmenopausal Osteoporosis Excipients Q.S. — Disintegrant / Filler Alfacalcidol Softgel Capsules
FreeProduct Composition & Strength
We supply this product as a Liquid-Filled Soft Gelatin Capsule, packed in highly protective, opaque blister strips to prevent the extreme light-degradation associated with vitamin D analogues.
Active Ingredient Strength Primary Clinical Use Alfacalcidol BP/EP 0.25 mcg (Micrograms) Initial Titration / Pediatric / Maintenance Dosing Alfacalcidol BP/EP 0.5 mcg (Micrograms) Standard Adult Dialysis / Osteoporosis Dosing Alfacalcidol BP/EP 1.0 mcg (Micrograms) Severe Hypocalcemia / High-PTH Suppression Excipients Refined Arachis (Peanut) Oil / BHA Lipid Carrier System / Antioxidant Stabilizer *Pack Sizes: 10×10 Opaque Alu-PVC Blisters or Alu-Alu Blisters. (Opaque packaging is an absolute necessity to maintain microgram API stability).
Allopurinol Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration).
Active Ingredient Strength (Standard) Role Allopurinol IP/BP/USP 100 mg Initial Dose / Renal Adjustment Allopurinol IP/BP/USP 300 mg Standard Maintenance Dose Excipients Q.S. Binder / Disintegrant Altretamine Capsules
FreeAltretamine capsules are antineoplastic (chemotherapy) medications used primarily for the palliative treatment of advanced ovarian cancer. They are most commonly available in a 50 mg strength.
Aluminium hydroxide Magnesium Trisilicate Tablet
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (Mint/Orange Flavor). The chewable format is essential to increase the surface area for rapid reaction.
Active Ingredient Strength (Standard) Role Dried Aluminium Hydroxide Gel USP/BP 250 mg Acid Neutralizer / Astringent Magnesium Trisilicate USP/BP 500 mg Acid Neutralizer / Adsorbent Excipients Q.S. Mannitol / Menthol (Flavor) Amikacin Sulphate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid in Glass Vials or Ampoules. The solution is clear, colorless to pale yellow, and requires no reconstitution (ready-to-use).
ant Active Ingredient Strength (Standard) Therapeutic Role Amikacin Sulphate USP/BP 100 mg / 2 ml Pediatric Dose Amikacin Sulphate USP/BP 250 mg / 2 ml Intermediate Dose Amikacin Sulphate USP/BP 500 mg / 2 ml Adult Standard Dose Excipients Q.S. Sodium Citrate / Sodium Metabisulfite Buffer / Antioxid *Pack Sizes: Tray of 10 Ampoules or Box of 1/10 Vials.
Amiodarone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. The formulation utilizes specific co-solvents to solubilize the lipophilic Amiodarone molecule.
Active Ingredient Strength (Standard) Therapeutic Role Amiodarone HCl BP/USP 150 mg / 3 ml (50 mg/ml) Antiarrhythmic Agent Vehicle / Solvents Q.S. Polysorbate 80 / Benzyl Alcohol Solubilizing Agents *Pack Sizes: Tray of 5 Ampoules or 10 Ampoules.
Amiodarone Tablet
FreeProduct Composition & Available Strengths
We manufacture Amiodarone in standard, internationally recognized strengths to allow for the intensive loading phase and lower maintenance doses required in cardiology.
Active Ingredient Standard Strengths Primary Clinical Target Amiodarone HCl BP / IP / USP 100 mg Low-Dose Maintenance: For fine-tuned long-term rhythm control and geriatric titration. Amiodarone HCl BP / IP / USP 200 mg Standard Therapy: Used for initial institutional oral loading phases and standard daily maintenance. Amitriptyline Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often Blue, Yellow, or Orange depending on strength) to mask the intensely bitter taste of the API.
Active Ingredient Strength (Standard) Primary Role Amitriptyline HCl IP/BP/USP 10 mg Neuropathic Pain / Migraine / Sleep Amitriptyline HCl IP/BP/USP 25 mg Pain / Depression Initiation Amitriptyline HCl IP/BP/USP 50 mg Major Depression (Maintenance) Amitriptyline HCl IP/BP/USP 75 mg High Potency / Severe Depression Amlodipine Tablet
FreeAmlodipine Tablets IP 5 mg
Each Uncoated tablet contains :
Amlodipine Besylate IP
Eq to Amlodipine 5 mgAmlodipine Tablets IP 10 mg
Each Uncoated Tablet Contains :
Amlodipine Besylate IP
Eq To Amlodipine 10 mgAmlodipine Besylate Tablets IP 2.5 mg
Each uncoated tablet contains :
Amlodipine Besylate IP
Eq. To Amlodipine 2.5 mgAmlodipine Besylate Tablets IP 2.5 mg
Each Film Coated Tablet Contains:
Amlodipine Besylate IP
eq. To Amlodipine 2.5 mgAmlodipine Besylate Tablets IP 5 mg
Each Film Coated Tablet Contains:
Amlodipine Besylate IP
eq. To Amlodipine 5 mgAMLODIPINE & ENALAPRIL MALEATE TABLET
Each Film Coated Tablet Contains :
Amlodipine Besylate
Eq. To Amlodipine 5 mg
Enalapril Maleate 5 mg
Excipients q.sAMLODIPINE & LISINOPRIL TABLET
Each Film Coated Tablet Contains :
Amlodipine Besylate
Eq. To Amlodipine 5 mg
Lisinopril dihydrate
Eq. To Lisinopril 5 mg
Excipients q.sTRIPPLEACE AMLODIPINE -10 / AMLODIPINE
TABLETS 10 MG
Each uncoated tablet contains:
Amlodipine Besilate BP
Equivalent to Amlodipine 10 mg
Excipients Q.S.Usage: – Treat high blood pressure
Category: – Hypertensive / Cardiac Drugs
Therapeutic category: – hypertensive, Cardiovascular Agent,
Amodiaquine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Yellow) or Film Coated Tablets. The strength is typically expressed in terms of the Amodiaquine Base.
Active Ingredient Strength (Base Equivalent) Salt Content (Approx) Role Amodiaquine HCl USP/BP 67.5 mg ~ 90 mg Pediatric (ACT Component) Amodiaquine HCl USP/BP 153 mg / 150 mg ~ 200 mg Adolescent / Co-blistered Amodiaquine HCl USP/BP 200 mg ~ 260 mg Standard Adult Dose Excipients Q.S. Microcrystalline Cellulose / Magnesium Stearate Direct Compression Amoxicillin & Potassium Clavulanate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, ultra-low moisture Alu-Alu blister strips (often containing integrated desiccants) to ensure the absolute stability of the incredibly hygroscopic Clavulanate salt.
Active Ingredient Strength Primary Clinical Function Amoxicillin Trihydrate USP/Ph.Eur.
Potassium Clavulanate USP/Ph.Eur.500 mg
125 mg
(Total: 625 mg)Standard Adult Dose: Therapy for moderate RTIs, dental infections, and skin infections. Amoxicillin Trihydrate USP/Ph.Eur.
Potassium Clavulanate USP/Ph.Eur.875 mg
125 mg
(Total: 1000 mg)High-Dose Adult Therapy: Aggressive intervention for severe pneumonia, severe sinus infections, and bite wounds. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Moisture Scavenger (Engineered for immediate gastric dissolution) *Pack Sizes: 1×6 or 1×10 Alu-Alu Blisters (Optimized specifically for strict 5-to-7 day acute antibiotic regimens).
Amoxicillin Capsules
FreeAmoxicillin capsules are common penicillin-type antibiotics typically available in 250 mg and 500 mg strengths.
Amoxicillin Sodium Injection 250mg
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Pediatric Dose) Therapeutic Role Amoxicillin Sodium USP/BP Equivalent to 250 mg Amoxicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Amoxicillin Sodium Injection 500mg
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard Adult Dose) Therapeutic Role Amoxicillin Sodium USP/BP Equivalent to 500 mg Amoxicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Amoxycillin & Cloxacillin Capsules
FreeAmoxycillin and cloxacillin capsules (commonly known as co-amoxiclox) are combination antibiotics used to treat infections where bacteria might produce enzymes that resist standard penicillin. They are typically available in a 500 mg total strength (250 mg / 250 mg)
Amoxycillin & Dicloxacillin Capsules
FreeAmoxycillin and dicloxacillin capsules are combination antibiotics designed to broaden the spectrum of treatment while protecting the medicine from bacterial resistance. They are typically available in a 500 mg total strength (often 250 mg / 250 mg)
Amoxycillin & Potassium Clavulanate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The ratio is critically balanced (usually 5:1) for optimal pharmacokinetics in intravenous use.
Strength Variant Amoxicillin Content (as Sodium) Clavulanic Acid Content (as Potassium) Target Patient 1.2 g Vial 1000 mg (1 g) 200 mg Adults (Severe) 600 mg Vial 500 mg 100 mg Adults / Children 300 mg Vial 250 mg 50 mg Pediatric 150 mg Vial 125 mg 25 mg Infants *Pack Sizes: Tray of 1 Vial or Box of 1/10 Vials with Water for Injection (WFI).
Amoxycillin Capsules
FreeAmoxycillin capsules are widely used penicillin-type antibiotics. They are most frequently prescribed in 250 mg and 500 mg strengths.Ampicillin & Cloxacillin Capsules
FreeAmpicillin and cloxacillin capsules (often called co-ampiclox) are combination antibiotics used to treat infections where the bacteria may produce enzymes that destroy standard penicillin. They are most commonly available in a 500 mg total strength (250 mg / 250 mg)
Ampicillin & Cloxacillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard 1:1 Ratio) Therapeutic Role Ampicillin Sodium USP/BP 250 mg Broad Spectrum Coverage Cloxacillin Sodium USP/BP 250 mg Anti-Staphylococcal Shield Total Vial Strength 500 mg Pediatric / Mild Infection (Adult Variant) 500 mg Ampicillin + 500 mg Cloxacillin (1 g Total) Standard Adult Dose Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ampicillin & Dicloxacillin Capsules
FreeAmpicillin and dicloxacillin capsules are combination antibiotics designed to provide broad-spectrum coverage while resisting degradation by certain bacterial enzymes. They are commonly available in a 500 mg total strength (typically 250 mg / 250 mg).
Ampicillin and Flucloxacillin Capsules
FreeAmpicillin and flucloxacillin capsules (often referred to by the co-drug name co-fluampicil) are combination antibiotics used to treat infections where the specific bacteria is unknown or suspected to be a penicillin-resistant strain. They are typically available in a 250 mg/250 mg strength.
Ampicillin Capsules
FreeAmpicillin capsules are a penicillin-type antibiotic used to treat various bacterial infections. They are most commonly available in 250 mg and 500 mg strengths.
Ampicillin Injection 1gm
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard Adult Dose) Therapeutic Role Ampicillin Sodium USP/BP Equivalent to 1000 mg (1 g) Ampicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ampicillin Injection 500mg
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard Pediatric/Mild Dose) Therapeutic Role Ampicillin Sodium USP/BP Equivalent to 500 mg Ampicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ampicillin Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The 2:1 ratio is clinically optimized for pharmacokinetics.
Active Ingredient Strength (Standard 1.5g Vial) Strength (High Dose 3g Vial) Ampicillin Sodium USP/BP 1000 mg (1 g) 2000 mg (2 g) Sulbactam Sodium USP/BP 500 mg (0.5 g) 1000 mg (1 g) Total Vial Content 1.5 g 3.0 g Excipients None (Pure Sterile Powder) None (Pure Sterile Powder) *Pack Sizes: Tray of 10 Vials, or Box of 1 Vial with Water for Injection (WFI).
Arteether Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules. The oily base (refined Arachis Oil or Ethyl Oleate) ensures depot formation in the muscle.
Active Ingredient Strength (Standard) Therapeutic Role α-β Arteether 150 mg / 2 ml Adult Dose (Standard) α-β Arteether 75 mg / 1 ml Pediatric Dose Vehicle Q.S. Refined Arachis Oil / Ethyl Oleate Oily Base (Sustained Release) *Pack Sizes: Tray of 3 Ampoules (Full Course) or Box of 10 Ampoules.
Artemether & Lumefantrine Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Yellow) or Dispersible Tablets (Sweetened for Pediatrics). The standard regimen is a fixed ratio of 1:6.
Strength Variant Artemether Content Lumefantrine Content Target Patient Standard / Pediatric 20 mg 120 mg Infants & Children (5kg–35kg) Double Strength (DS) 40 mg 240 mg Adolescents / Simplified Dosing Adult Forte (80/480) 80 mg 480 mg Adults (>35kg) – High Compliance Artemether 40mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules. The oily base ensures a depot effect for sustained release.
Active Ingredient Strength (Standard) Therapeutic Role Artemether IP/Ph.Int 40 mg / 1 ml Pediatric / Low Body Weight Dose Artemether IP/Ph.Int 80 mg / 1 ml Adult Standard Dose Vehicle Q.S. Refined Arachis Oil / Ethyl Oleate Oily Base (Depot) *Pack Sizes: Tray of 6 Ampoules or 10 Ampoules (Standard Course).
Artemether-80 Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules. The 80mg strength is specifically formulated to minimize the injection volume for adult patients while delivering a potent therapeutic dose.
Active Ingredient Strength (Adult Dose) Therapeutic Role Artemether IP/Ph.Int 80 mg Potent Antimalarial Vehicle Q.S. to 1 ml Refined Arachis Oil / Ethyl Oleate *Pack Sizes: Tray of 6 Ampoules or 10 Ampoules (Standard Adult Course).
Artesunate 120mg Injection
FreeProduct Composition & Strength
We supply this product as a Combi-Pack containing the Lyophilized Powder and special solvents required for activation.
Component Content Function Vial (Powder) Artesunate 120 mg (Sterile Lyophilized) Active Antimalarial Ampoule 1 Sodium Bicarbonate Injection (5%) – 1ml Activator / Solvent (Solubilizes the acid) Ampoule 2 Sodium Chloride Injection (0.9%) – 5ml Diluent (Adjusts volume/tonicity) *Pack Sizes: Single Combi-Pack or Tray of 5 Combi-Packs.
Artesunate 30mg Injection
FreeProduct Composition & Strength
We supply this product as a Combi-Pack containing the Lyophilized Powder and special solvents required for activation.
Component Content Function Vial (Powder) Artesunate 30 mg (Sterile Lyophilized) Active Antimalarial Ampoule 1 Sodium Bicarbonate Injection (5%) – 0.5ml Activator (Solubilizes the acid) Ampoule 2 Sodium Chloride Injection (0.9%) – 2.5ml Diluent (Adjusts volume/tonicity) *Pack Sizes: Single Combi-Pack or Tray of 5/10 Combi-Packs.
Artesunate 60mg Injection
FreeProduct Composition & Strength
We supply this product as a Combi-Pack containing the Lyophilized Powder and special solvents required for activation.
Component Content Function Vial (Powder) Artesunate 60 mg (Sterile Lyophilized) Active Antimalarial Ampoule 1 Sodium Bicarbonate Injection (5%) – 0.5ml/1ml Activator (Solubilizes the acid) Ampoule 2 Sodium Chloride Injection (0.9%) – 2.5ml/5ml Diluent (Adjusts volume/tonicity) *Pack Sizes: Single Combi-Pack or Tray of 5 Combi-Packs.
Artesunate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. Stability is a key factor in our formulation.
Active Ingredient Strength (Standard) Role Artesunate IP/BP 50 mg Pediatric / Initial Dose Artesunate IP/BP 100 mg Adult Standard Dose Artesunate IP/BP 200 mg High Strength (Combination Protocols) Ascorbic Acid Tablet
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (Sugar/Sugar-Free) or Film Coated Tablets (Swallowable).
Active Ingredient Strength (Standard) Form Role Ascorbic Acid IP/BP/USP 100 mg Uncoated / Coated Pediatric / Maintenance Ascorbic Acid IP/BP/USP 500 mg Chewable (Orange) Standard Adult Dose Ascorbic Acid IP/BP/USP 1000 mg Chewable / Effervescent High Potency / Immunity Sodium Ascorbate Var. Buffered Salt Reduced Acidity Variant Atazanavir Capsules
FreeAtazanavir capsules are protease inhibitor antiretroviral medications used to treat HIV-1 infection. They are typically available in strengths of 150 mg, 200 mg, and 300 mg.
Atenolol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (often scored for dosage adjustment).
Active Ingredient Strength (Standard) Role Atenolol IP/BP/USP 25 mg Low Dose / Renal Impairment Atenolol IP/BP/USP 50 mg Standard Adult Dose Atenolol IP/BP/USP 100 mg High Potency / Angina Excipients Q.S. Binder / Disintegrant Atorvastatin Clopidogrel and Aspirin Capsules
FreeAtorvastatin, clopidogrel, and aspirin capsules are fixed-dose combination (FDC) medications used for the secondary prevention of cardiovascular events like heart attacks and strokes.
Atorvastatin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The active ingredient is used in the amorphous or crystalline form depending on bioavailability requirements.
Active Ingredient Strength (Standard) Role Atorvastatin Calcium IP/BP/USP 10 mg Primary Prevention / Maintenance Atorvastatin Calcium IP/BP/USP 20 mg Standard Therapeutic Dose Atorvastatin Calcium IP/BP/USP 40 mg High Intensity Therapy Atorvastatin Calcium IP/BP/USP 80 mg Acute Coronary Syndrome Atropine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Clear Glass Ampoules.
Active Ingredient Strength (Standard) Therapeutic Role Atropine Sulphate USP/BP 0.6 mg / ml Pre-operative / Cardiac Dose Atropine Sulphate USP/BP 1 mg / ml Emergency / Antidote Dose Excipients Q.S. Sodium Chloride / Sulfuric Acid (pH adjustment) Isotonicity / Stabilizer *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules (Hospital/Military Pack).
Azathioprine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Yellow/Pale Yellow) in blister packs or bulk containers.
Active Ingredient Strength (Standard) Role Azathioprine USP/BP 50 mg Standard Adult Dose Azathioprine USP/BP 25 mg Low Dose / Renal Adjustment Excipients Q.S. Binder / Coating Agent Azithromycin Dispersible Tablet
FreeProduct Composition & Strength
We supply this product as Dispersible Tablets (DT) with advanced taste-masking technology.
Active Ingredient Strength Flavor Profile Role Azithromycin IP/BP/USP 100 mg Orange / Peppermint Pediatric Low Dose Azithromycin IP/BP/USP 250 mg Orange / Peppermint Pediatric Standard / Adult Excipients Q.S. Sweeteners Disintegrant / Flavor Azithromycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Infusion in glass vials. It must be reconstituted and further diluted before administration.
Active Ingredient Strength (Standard Adult Dose) Therapeutic Role Azithromycin (as Dihydrate/Citrate) Equivalent to 500 mg Azithromycin Broad Spectrum Macrolide Excipients Q.S. Citric Acid / Sodium Hydroxide pH Adjuster / Solubilizer *Pack Sizes: Tray of 1 Vial, 5 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Azithromycin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential to mask the extremely bitter taste and facilitate swallowing.
Active Ingredient Strength (Standard) Standard Regimen Primary Role Azithromycin Dihydrate USP/BP 250 mg 6 Tablets (3-5 Days) Step-down Therapy / Pediatric Azithromycin Dihydrate USP/BP 500 mg 3 Tablets (3 Days) Respiratory Infections / Typhoid Azithromycin Dihydrate USP/BP 1000 mg (1 g) 1 Tablet (Single Dose) STI (Chlamydia / Gonorrhea) Excipients Q.S. Pregelatinized Starch / HPMC Disintegration / Coating Benzathine Penicillin Injection 1.2 MIU
FreeProduct Composition & Strength
We supply this product as a Sterile Powder for Suspension in glass vials. It requires reconstitution with Sterile Water for Injection to form a milky white suspension.
Active Ingredient Strength (International Units) Therapeutic Role Benzathine Penicillin G USP/BP 1,200,000 IU (1.2 MIU) Standard Adult Prophylaxis Excipients Q.S. Lecithin / Sodium Citrate Suspending / Buffering Agents *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Benzathine Penicillin Injection 2.4 MIU
FreeProduct Composition & Strength
We supply this product as a Sterile Powder for Suspension in glass vials. It requires reconstitution with Sterile Water for Injection to form a milky white suspension.
Active Ingredient Strength (International Units) Therapeutic Role Benzathine Penicillin G 1,200,000 IU (1.2 MIU) Pediatric / Standard Dose Benzathine Penicillin G 2,400,000 IU (2.4 MIU) Adult Syphilis / High Dose Benzathine Penicillin G 600,000 IU (0.6 MIU) Pediatric Prophylaxis Excipients Q.S. Lecithin / Sodium Citrate Suspending / Buffering Agents *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Benzhexol Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets. The chemical name Benzhexol and Trihexyphenidyl refer to the exact same molecule.
Active Ingredient Strength (Standard) Role Trihexyphenidyl HCl (Benzhexol) 2 mg Initial Dose / Mild EPS Trihexyphenidyl HCl (Benzhexol) 5 mg Forte / Maintenance Dose Excipients Q.S. Binder / Filler Benzyl Penicillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Buffered Powder for Injection in glass vials. The potency is measured in International Units (IU).
Active Ingredient Strength (IU) Mass Equivalent Therapeutic Role Benzyl Penicillin Sodium 1,000,000 IU (1 MU) ~600 mg Standard Dose Benzyl Penicillin Sodium 5,000,000 IU (5 MU) ~3000 mg High Dose (Meningitis) Benzyl Penicillin Sodium 10,000,000 IU (10 MU) ~6000 mg Severe Sepsis Buffering Agent Sodium Citrate – pH Stabilizer *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Betamethasone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Clear Glass Ampoules. The phosphate ester ensures high water solubility and rapid onset of action.
Active Ingredient Strength (Standard) Therapeutic Role Betamethasone Sodium Phosphate USP/BP Equivalent to 4 mg Betamethasone Potent Anti-inflammatory Excipients Q.S. Disodium Edetate / Sodium Metabisulfite Stabilizer / Antioxidant *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules (Hospital Pack)
Biperiden Tablets
FreeProduct Composition & Strength
We supply this product as Tablets (usually White, scored). The 2 mg strength is the global standard for titration.
Active Ingredient Strength (Standard) Primary Role Biperiden Hydrochloride USP/BP 2 mg Standard Therapeutic Dose Excipients Q.S. Lactose Monohydrate / Maize Starch Filler / Binder Bisacodyl Tablets
FreeProduct Composition & Strength
We supply this product as Enteric Coated Tablets (Gastro-resistant). The specialized coating is non-negotiable to prevent gastric irritation.
Active Ingredient Strength (Standard) Formulation Type Primary Role Bisacodyl USP/BP 5 mg Enteric Coated (Sugar or Film) Standard Adult Dose Bisacodyl USP/BP 10 mg Enteric Coated Strong Dose / Bowel Prep Excipients Q.S. Methacrylic Acid Copolymer (Enteric) pH-Dependent Release Bisoprolol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (distinctively shaped/scored). The low-dose range is critical for the “Start Low, Go Slow” titration required in heart failure.
Active Ingredient Strength (Standard) Shape/Color Primary Role Bisoprolol Fumarate USP/BP 2.5 mg White (Scored) Heart Failure Initiation Bisoprolol Fumarate USP/BP 5 mg Yellow/Pink (Scored) Standard Hypertension Bisoprolol Fumarate USP/BP 10 mg Orange/White High Dose Maintenance Excipients Q.S. Microcrystalline Cellulose / Hypromellose Filler / Coating Bleomycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder in glass vials. Potency is measured in USP Units, not milligrams.
Active Ingredient Strength Therapeutic Role Bleomycin Sulphate USP/IP 15 Units (approx. 15 mg) Antineoplastic Antibiotic Excipients Nitrogen (Inert Atmosphere) None (Pure Powder) *Pack Sizes: Single Vial Box or Tray of 10 Vials.
Bortenat
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder in glass vials. It must be reconstituted with Normal Saline (0.9% NaCl).
Active Ingredient Strength Reference Brand Bortezomib (as Mannitol Ester) 2 mg / Vial Bortenat 2mg Bortezomib (as Mannitol Ester) 3.5 mg / Vial Bortenat 3.5mg Excipients Mannitol USP/BP Stabilizer *Pack Sizes: Single Vial Box with protective Cytotoxic shrink-wrapping.
Bortezomib Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder in glass vials. It contains Mannitol, which forms a stable boronic ester with Bortezomib for shelf stability.
Active Ingredient Vial Strength Primary Use Bortezomib (as Mannitol Boronic Ester) 2 mg / Vial Single Dose / Low BSA Bortezomib (as Mannitol Boronic Ester) 3.5 mg / Vial Standard Adult Dose Excipients Mannitol (Sterile) Stabilizer / Bulking Agent *Pack Sizes: Single Vial Box with protective Cytotoxic shrink-wrapping.
ortezomib injection is an antineoplastic (cancer) medication supplied as a sterile lyophilised powder (freeze-dried cake) for reconstitution. It is most commonly known by the brand name Velcade.
Bromocriptin Tablets
FreeBromocriptin Mesylate Tablets IP 2.5 MG
Each uncoated tablet contains
Bromocriptin Mesylate IP
eq.to Bromocriptine 2.5 mgUsage: – high levels of a natural substance prolactin in the body
Category: – Anti Parkinson drugs
Therapeutic category: – Anti Parkinson
Bupivacaine Hydrochloride In Dextrose Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Hyperbaric Solution in 4ml Glass Ampoules.
Active Ingredient Strength Function Bupivacaine Hydrochloride USP/BP 0.5% w/v (5 mg/ml) Local Anesthetic (Long Acting) Dextrose (Monohydrate) 8% w/v (80 mg/ml) Baricity Adjuster (Makes it Heavy) *Pack Sizes: Tray of 5 Ampoules or 50 Ampoules (Hospital Pack).
Bupivacaine Injection
FreeBupivacaine hydrochloride injection is a sterile, isotonic solution of a long-acting amide-type local anaesthetic. It is available in various concentrations and formulations depending on whether it contains preservatives or vasoconstrictors like epinephrine.
Calcium & Chloecalciferol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Swallowable) or Chewable Tablets (Flavor masked). The chewable format is popular due to the large size of calcium tablets.
Component Strength (Standard) Strength (High Potency) Role Elemental Calcium
(from Calcium Carbonate)500 mg
(1250 mg Salt)500 mg
(1250 mg Salt)Bone Mineralization Vitamin D3
(Cholecalciferol)250 IU 500 IU / 1000 IU Absorption Enhancer Excipients Q.S. Starch / Povidone Binding Agent Calcium Carbonate & Vitamin D3 Tablets
FreeProduct Composition & Common Strengths
We supply this combination in standard, clinically calibrated ratios designed to optimize daily absorption thresholds without overwhelming intestinal transit.
Active Ingredient Components Standard Strengths (per Tablet) Elemental Yield / Biological Activity Primary Clinical Function Calcium Carbonate IP / BP / USP 1250 mg Yields 500 mg Elemental Calcium The Scaffold: Provides the physical structural block for bone density. Vitamin D3 (Cholecalciferol) IP/BP/USP 250 IU / 400 IU Equivalent to 6.25 mcg / 10.0 mcg The Catalyst: Chemically drives intestinal transport channels. Excipients Pharma Grade Modified Matrix Adjusters The Carrier: Ensures fast disintegration or chewable palatability. Calcium Citrate With Vitamin D3 Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Off-White, Oblong/Caplet shape). The coating makes the large tablet easier to swallow.
Active Ingredient Strength (Standard) Therapeutic Role Calcium Citrate USP/BP 1000 mg (Eq. to 210 mg Elemental Ca) Bone Mineralization Vitamin D3 (Cholecalciferol) USP/BP 200 IU / 400 IU / 1000 IU Absorption Enhancer (High Strength Variant) 1200 mg Citrate + 1000 IU D3 Severe Osteoporosis Excipients Q.S. Starch / Magnesium Stearate / HPMC Disintegrant / Coating Calcium Citrate,Vitamin D3, Magnesium, Zinc Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Blue, Oblong). The coating masks the metallic taste of Zinc and Magnesium.
Active Ingredient Strength (Standard) Therapeutic Role Calcium Citrate USP/BP 1000 mg (Eq. to 210 mg Elemental Ca) Bone Mineralization Vitamin D3 (Cholecalciferol) 200 IU / 400 IU Absorption Enhancer Magnesium Hydroxide USP/BP 100 mg (Eq. to Elemental Mg) D3 Activation / Bone Structure Zinc Sulphate Monohydrate USP/BP 4 mg / 10 mg (Eq. to Elemental Zn) Collagen Synthesis Excipients Q.S. Croscarmellose Sodium / HPMC Disintegrant / Coating Calcium Dobesilate Capsules
FreeCalcium dobesilate capsules are vasoprotective medications primarily used to treat chronic venous insufficiency and diabetic retinopathy. They are most commonly available in a 500 mg strength
Calcium Gluconate Injection
FreeProduct Composition & Strength
We supply this product as a Supersaturated Sterile Solution in 10ml ampoules.
Active Ingredient Concentration Elemental Calcium Content Calcium Gluconate Monohydrate USP/BP 10% w/v (100 mg / ml) 0.465 mEq/ml (Approx 9 mg Ca++ / ml) Stabilizer Calcium D-Saccharate Prevents Crystallization *Pack Sizes: Tray of 10 Ampoules (10ml) or 50 Ampoules.
Calcium Gluconate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Chewable Tablets in bulk jars or blisters.
Active Ingredient Strength Elemental Calcium Role Calcium Gluconate IP/BP/USP 500 mg ~ 45 mg Pediatric / Maintenance Calcium Gluconate IP/BP/USP 1000 mg (1g) ~ 90 mg Adult Therapeutic Dose Excipients Q.S. — Binder / Sweetener Candesartan Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). The wide range of strengths allows for precise titration in heart failure patients.
Active Ingredient Strength (Standard) Primary Role Candesartan Cilexetil USP/BP 4 mg Heart Failure Initiation / Hepatic Impairment Candesartan Cilexetil USP/BP 8 mg Standard Hypertension Start Candesartan Cilexetil USP/BP 16 mg Standard Maintenance Candesartan Cilexetil USP/BP 32 mg High Dose / Resistant Hypertension Carbamazepine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (White, scored). We also offer Controlled Release (CR) variants upon request.
Active Ingredient Strength (Standard) Primary Role Carbamazepine USP/BP 100 mg Pediatric / Initiation Dose Carbamazepine USP/BP 200 mg Standard Adult Dose Carbamazepine USP/BP 400 mg High Dose / CR Formulation Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Carbidopa and Levodopa Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (often scored/mottled). The ratios are designed to minimize nausea while maximizing brain dopamine levels.
Carbidopa (Anhydrous) Levodopa Ratio Primary Role 10 mg 100 mg 1:10 Low Dose Initiation 25 mg 100 mg 1:4 Standard Maintenance (Best Nausea Control) 25 mg 250 mg 1:10 High Dose / Advanced Disease Excipients Q.S. Microcrystalline Cellulose / Starch / Dye Filler / Colorant Carboplatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid Concentrate in glass vials. It is ready to dilute.
Active Ingredient Concentration Vial Size (Total Drug) Carboplatin USP/BP 10 mg / ml 150 mg (15 ml vial) Carboplatin USP/BP 10 mg / ml 450 mg (45 ml vial) Excipients Water for Injection / Mannitol – *Pack Sizes: Single Vial Box with protective Cytotoxic shrink-wrapping.
Carvedilol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. Because therapy for Heart Failure requires very precise “low dose” initiation, we offer the full titration range.
Active Ingredient Strength (Standard) Color Code (Typical) Role Carvedilol USP/BP 3.125 mg White/Pink CHF Initiation (Critical) Carvedilol USP/BP 6.25 mg Yellow Titration Step 1 Carvedilol USP/BP 12.5 mg Tan/Peach Titration Step 2 Carvedilol USP/BP 25 mg White Target Maintenance Dose Cefadroxil 500 mg Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant Alu-Alu or High-Density Alu-PVC blister strips to ensure the absolute stability of the beta-lactam ring.
Active Ingredient Strength Primary Clinical Function Cefadroxil Monohydrate USP/Ph.Eur. 500 mg (Equivalent to anhydrous Cefadroxil) Global Standard: Twice-daily adult therapy for pharyngitis, skin infections, and UTIs. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Macrogol / Magnesium Stearate Diluent / Superdisintegrant / Film-Coating (Engineered for rapid gastric dissolution and high bioavailability) Cefazolin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard) Therapeutic Role Cefazolin Sodium USP/BP Equivalent to 1000 mg (1 g) Cefazolin Adult Surgical Dose Cefazolin Sodium USP/BP Equivalent to 500 mg Cefazolin Pediatric / Mild Infection Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefepime Content Sulbactam Content Ratio 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) 2:1 (Standard) Excipients L-Arginine Buffer / Stabilizer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefepime Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients L-Arginine Buffer / Stabilizer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains L-Arginine as a buffering agent (instead of sodium salts).
Active Ingredient Strength Therapeutic Role Cefepime Hydrochloride USP/BP Equivalent to 1000 mg (1 g) Cefepime Severe Infection / Sepsis Cefepime Hydrochloride USP/BP Equivalent to 500 mg Cefepime Pediatric / Moderate Infection Buffer L-Arginine pH Stabilizer (Approx 725 mg per g) *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefixime Capsules 400mg
FreeCefixime 400mg capsules are third-generation cephalosporin antibiotics used for a variety of bacterial infections. While 200mg is a common dose, the 400mg strength is often used for once-daily dosing.
Cefoperazone & Sulbactam 2Gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in 20ml glass vials.
Active Ingredient Strength Function Cefoperazone Sodium USP/BP 1000 mg (1 g) Anti-Pseudomonal Cephalosporin Sulbactam Sodium USP/BP 1000 mg (1 g) Beta-Lactamase Inhibitor Ratio 1 : 1 High Sulbactam Load *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with 10ml Water for Injection (WFI).
Cefoperazone & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 1:1.
Strength Variant Cefoperazone Content Sulbactam Content Ratio 1.5 g Vial 500 mg (Sodium) 500 mg (Sodium) 1:1 (Standard) 3.0 g Vial 1000 mg (1 g) 1000 mg (1 g) 1:1 (High Dose) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefoperazone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefoperazone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – Cefoperazone Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approximately 34 mg (1.5 mEq) of sodium per gram.
Active Ingredient Strength (Standard) Therapeutic Role Cefoperazone Sodium USP/BP Equivalent to 1000 mg (1 g) Cefoperazone Adult Surgical / Biliary Dose Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefotaxime Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The sodium content is lower than many other cephalosporins (approx 2.2 mmol/g).
Active Ingredient Strength Primary Patient Cefotaxime Sodium USP/BP Equivalent to 1000 mg (1 g) Adults (Meningitis/Sepsis) Cefotaxime Sodium USP/BP Equivalent to 500 mg Pediatrics Cefotaxime Sodium USP/BP Equivalent to 250 mg Neonates / Infants Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefpirome & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefpirome Content (as Sulfate) Sulbactam Content (as Sodium) Ratio 1.5 g Vial 1000 mg (1 g) 500 mg 2:1 (Standard) Excipients Sodium Carbonate Buffer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefpirome Sulfate Injection
FreeCefpirome sulfate injection is a fourth-generation cephalosporin antibiotic typically supplied as a sterile dry powder for intravenous (IV) or intramuscular (IM) administration
Ceftazidime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is either 2:1 or 1:1 depending on the market requirement.
Strength Variant Ceftazidime Content Sulbactam Content Ratio 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) 2:1 (Standard) 2.25 g Vial 1125 mg 1125 mg 1:1 (High Potency) Excipients Sodium Carbonate Buffer – *Pack Sizes: Tray of 1 Vial or Box of 1/10 Vials with Water for Injection (WFI).
Ceftazidime & Tazobactam Injection
FreeCeftazidime and tazobactam injection is a combination antibiotic used primarily in hospital settings for serious, multi-drug resistant bacterial infections. It is typically available as a sterile dry powder for reconstitution.
Product Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Ceftazidime Content Tazobactam Content Target Patient 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) Standard Adult Dose 281.25 mg Vial 250 mg 31.25 mg Pediatric Dose Excipients Sodium Carbonate Buffer Solubilizer Ceftazidime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains Sodium Carbonate as a solubilizer.
Active Ingredient Strength Primary Patient Ceftazidime Pentahydrate USP/BP Equivalent to 1000 mg (1 g) Adults (Standard Dose) Ceftazidime Pentahydrate USP/BP Equivalent to 250 mg Pediatrics / Neonates Excipients Sodium Carbonate Gas-Releasing Buffer *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftizoxime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approx. 2.6 mEq (60 mg) of sodium per gram.
Active Ingredient Strength Primary Use Ceftizoxime Sodium USP/BP Equivalent to 1000 mg (1 g) Ceftizoxime Severe Infection / Anaerobic Ceftizoxime Sodium USP/BP Equivalent to 500 mg UTI / Gonorrhea Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone & Sulbactam injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Ceftriaxone Content Sulbactam Content Target Patient 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) Adult Standard Dose 750 mg Vial 500 mg 250 mg Pediatric / Moderate Dose 375 mg Vial 250 mg 125 mg Infant / Neonate Dose Ratio 2 : 1 – Optimal Synergy *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Ceftriaxone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) 562.5 mg Vial 500 mg 62.5 mg Pediatric Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone 1gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Standard Use Ceftriaxone Sodium USP/BP Equivalent to 1000 mg (1 g) Ceftriaxone Adult Standard Dose Sodium Content Approx 83 mg (3.6 mEq) Per 1g Vial *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone 500mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Target Use Ceftriaxone Sodium USP/BP Equivalent to 500 mg Ceftriaxone Pediatrics / IM Gonorrhea Sodium Content Approx 41.5 mg (1.8 mEq) Low Sodium Load *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefuroxime Content Sulbactam Content Primary Use 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) Adult Therapy / Surgery 1.125 g Vial 750 mg 375 mg Moderate Infection 375 mg Vial 250 mg 125 mg Pediatrics *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cefuroxime Sodium USP/BP Equivalent to 750 mg Cefuroxime Standard Adult Dose Cefuroxime Sodium USP/BP Equivalent to 1500 mg (1.5 g) Severe Infections / Surgery Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Amorphous Solid Dispersion Tablet, packed exclusively in secure, moisture-resistant Alu-Alu blister strips to ensure the stability of the hygroscopic prodrug.
Active Ingredient Strength Primary Clinical Function Cefuroxime Axetil USP/Ph.Eur.
(Equivalent to Cefuroxime)250 mg The Pediatric & ENT Anchor: The definitive unit utilized for the treatment of Acute Otitis Media, Pharyngitis, and uncomplicated Urinary Tract Infections. Cefuroxime Axetil USP/Ph.Eur. 500 mg The Respiratory Macrodose: The high-efficacy therapeutic payload required for the management of Community-Acquired Pneumonia, Bronchitis, and early-stage Lyme Disease. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Sodium Lauryl Sulfate / Colloidal Silicon Dioxide / Premium Polymeric Film Diluent / Superdisintegrant / Solubilizer / Glidant / Film-Coating (Engineered specifically utilizing Amorphous Solid Dispersion Technology. Because crystalline Cefuroxime Axetil has near-zero bioavailability, our tablets are engineered to maintain the API in its highly-soluble amorphous state for maximum clinical cure rates). *Pack Sizes: 1×6, 1×10, or 10×10 Alu-Alu Blisters (Optimized specifically for strict 5-to-10 day acute curative regimens).
Celecoxib Capsules
FreeCelecoxib capsules are selective non-steroidal anti-inflammatory drugs (NSAIDs) used to manage pain and inflammation. They are commonly available in strengths of 50 mg, 100 mg, 200 mg, and 400 mg.
Cephalexin Capsules
FreeCephalexin capsules are a first-generation cephalosporin antibiotic used to treat various bacterial infections. They are typically available in strengths of 250 mg, 500 mg, and sometimes 333 mg or 750 mg.
Cephalothin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approximately 2.8 mEq (64 mg) of Sodium per gram.
Active Ingredient Strength Therapeutic Role Cephalothin Sodium USP/BP Equivalent to 1000 mg (1 g) Cephalothin Surgical Prophylaxis / Skin Infection Excipients Sodium Bicarbonate Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cetrizine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (White/scored). The tablets are scored to facilitate dose splitting for pediatric use.
Active Ingredient Strength (Standard) Primary Role Cetirizine HCl USP/BP/IP 5 mg Pediatric / Mild Allergy Cetirizine HCl USP/BP/IP 10 mg Standard Adult Dose Excipients Q.S. Lactose Monohydrate / Maize Starch Chlorambucil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Dose Cytotoxic Tablet, packed exclusively in light-shielded, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the sensitive aromatic mustard payload.
Active Ingredient Strength Primary Clinical Function Chlorambucil USP/Ph.Eur. 2 mg The Standard Hematology Anchor: The definitive unit utilized for chronic, daily maintenance and precise titration in CLL and low-grade lymphomas. Chlorambucil USP/Ph.Eur. 5 mg The Pulse-Dosing Payload: High-efficacy therapeutic payload utilized for “Pulse” therapy regimens or initial aggressive induction phases. Excipients Lactose Anhydrous / Colloidal Silicon Dioxide / Magnesium Stearate / Hypromellose / Titanium Dioxide / Premium Polymeric Film Diluent / Glidant / Lubricant / Protective Cytotoxic Shield (Engineered specifically utilizing an impenetrable film coat. This ensures the highly toxic, mutagenic API never comes into contact with the skin of the pharmacist or caregiver handling the medication). *Pack Sizes: 25-Tablet or 30-Tablet Bottles/Blisters (Optimized for oncology-specific treatment cycles).
Chloramphenicol Capsules
FreeChloramphenicol capsules are broad-spectrum antibiotic medications primarily containing the active ingredient chloramphenicol. They are typically available in strengths of 250 mg or 500 mg per capsule.
Chloramphenicol Sodium Succinate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials. It must be reconstituted before use.
Active Ingredient Strength Therapeutic Role Chloramphenicol Sodium Succinate USP/BP Equivalent to 1000 mg (1 g) Chloramphenicol Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Chlordiazepoxide Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (often Green or Yellow). The robust coating is essential to mask the intensely bitter taste of the API and protect the light-sensitive drug.
Active Ingredient Strength (Standard) Therapeutic Role Chlordiazepoxide HCl USP/BP 10 mg Mild Anxiety / Elderly / Taper End Chlordiazepoxide HCl USP/BP 25 mg Severe Anxiety / Alcohol Detox Loading Excipients Q.S. Sucrose / Talc / Calcium Carbonate Sugar Coating (Light Barrier) Chloroquine Phosphate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Vials/Ampoules.
Active Ingredient Salt Strength Base Equivalent Chloroquine Phosphate USP/BP 64.5 mg / ml Equivalent to 40 mg Chloroquine Base Total Vial Content 30 ml Multi-dose Vial 1200 mg Base Total Excipients Chlorocresol (Preservative) Water for Injection *Pack Sizes: Tray of 10 Ampoules (5ml) or Multi-dose Vials (30ml).
Chloroquine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets or Uncoated Tablets. The strength is often labeled by the salt weight or the base equivalent.
Active Ingredient Salt Strength Base Equivalent (Active) Primary Role Chloroquine Phosphate USP/BP 250 mg 150 mg Base Pediatric / Prophylaxis Chloroquine Phosphate USP/BP 500 mg 300 mg Base Standard Adult Dose Excipients Q.S. Maize Starch / Magnesium Stearate Binder / Lubricant Chloroquine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is critical to mask the intensely bitter taste of the drug. Note: Dosing is often calculated based on the “Base” content.
Active Ingredient (Salt) Equivalent Base Primary Role Chloroquine Phosphate USP/BP 250 mg ~ 155 mg Base Prophylaxis / Maintenance Chloroquine Phosphate USP/BP 500 mg ~ 310 mg Base Acute Malaria Treatment Excipients Q.S. Starch / Magnesium Stearate Chlorphenamine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Therapeutic Role Chlorphenamine Maleate USP/BP 10 mg / ml Potent Antihistamine Excipients Sodium Chloride / Water for Injection Isotonicity Agent *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules (Hospital/ER Pack).
Chlorpromazine and Trihexyphenidyl Tablets
FreeProduct Composition & Strength
We supply this product in Precision-Blended configurations, often customized for institutional titration, packed in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips.
Active Ingredient Common Strengths Primary Clinical Function Chlorpromazine HCl USP/Ph.Eur. 25 mg / 50 mg / 100 mg The Antipsychotic Anchor: High-potency D2 blockade to control positive symptoms of psychosis and induce behavioral calm. Trihexyphenidyl HCl USP/Ph.Eur. 2 mg The Anti-Tremor Shield: Centrally acting anticholinergic required to neutralize drug-induced Parkinsonism and muscle rigidity. Excipients Lactose Monohydrate / Maize Starch / Povidone K-30 / Magnesium Stearate / Polymeric Film Coat Diluent / Binder / Disintegrant / Lubricant (Engineered specifically utilizing High-Shear Wet Granulation to ensure 100% uniformity of the 2mg Trihexyphenidyl payload alongside the larger Chlorpromazine dose, guaranteeing consistent motor protection). *Pack Sizes: 10×10 Blisters or Bulk Jars of 1000 (Optimized specifically for high-volume psychiatric hospital dispensing).
Chlorthalidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the stability of the micronized active ingredient.
Active Ingredient Strength Primary Clinical Function Chlorthalidone USP/BP 6.25 mg / 12.5 mg The Contemporary Starting Dose: Highly preferred for modern “Low-Dose” hypertension therapy to maximize pressure control while minimizing electrolyte loss. Chlorthalidone USP/BP 25 mg The High-Potency Payload: Utilized for resistant hypertension or the management of edema associated with heart failure or hepatic cirrhosis. Excipients Microcrystalline Cellulose / Colloidal Silicon Dioxide / Magnesium Stearate / Pregelatinized Starch Diluent / Glidant / Lubricant / Binder (Engineered specifically utilizing Micronized API Technology to ensure absolute uniformity in the 6.25mg and 12.5mg ultra-low-dose tablets, guaranteeing consistent renal response across every batch). Chlorzoxazone ,Ibuprofen & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as a High-Density, Precision-Compressed Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the stability of the large multi-API payload.
Active Ingredient Strength Primary Clinical Function Chlorzoxazone USP/BP 250 mg The Muscle Relaxant Anchor: Targets the spinal cord to inhibit the reflexes driving the muscle spasm. Ibuprofen USP/BP 400 mg The Anti-Inflammatory Payload: Blocks prostaglandin synthesis to reduce tissue swelling and peripheral pain. Paracetamol (Acetaminophen) USP/BP 325 mg The Central Analgesic Booster: Synergistically raises the pain threshold for rapid symptomatic relief. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Magnesium Stearate / Polymeric Film Coat Diluent / Superdisintegrant / Binder / Lubricant (Engineered specifically utilizing High-Pressure Rotary Compression to manage the massive ~1000mg tablet weight while ensuring the tablet remains swallowable and shatters instantly in gastric fluid). *Pack Sizes: 10×10 Blisters (Optimized specifically for 5-day to 10-day acute injury recovery cycles).
Cholecalciferol (Vitamin D3) Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in glass ampoules.
Active Ingredient Strength Vehicle Cholecalciferol USP/BP (Vitamin D3) 300,000 IU / 1 ml (7.5 mg) Oily Base (Arachis or Sesame Oil) Cholecalciferol USP/BP (Vitamin D3) 600,000 IU / 1 ml (15 mg) Oily Base (Arachis or Sesame Oil) Excipients BHT / Benzyl Alcohol Antioxidant / Preservative *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Cholecalciferol Granules Sachet
FreeProduct Composition & Strength
We supply this product as Free-Flowing Granules in 1-gram sachets (Single Dose). The granules are flavored (Orange/Lemon) to ensure palatability.
Active Ingredient Strength Formulation Base Role Cholecalciferol (Vitamin D3) IP/BP/USP 60,000 IU Stabilized Powder Deficiency Correction Excipients Q.S. to 1 gm Sucrose / Mannitol / Flavor Diluent / Taste Masking CILNIDIPINE & TELMISARTAN TABLETS
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bilayer or Co-Processed Tablet, packed exclusively in secure, high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive Telmisartan and light-sensitive Cilnidipine.
Active Ingredient Strength Primary Clinical Function Telmisartan USP/Ph.Eur. 40 mg The Hormonal Stabilizer: Blocks the RAAS system to provide 24-hour systemic pressure control and metabolic benefits (PPAR-gamma activation). Cilnidipine USP/Ph.Eur. 10 mg The Vascular Relaxant: Provides immediate N-type and L-type calcium channel blockade to lower peripheral resistance without edema. Excipients Meglumine / Sorbitol / Sodium Hydroxide / Magnesium Stearate / Titanium Dioxide (Opaque Coating) Solubilizer / Diluent / PH Modifier / Light Shield (Engineered specifically utilizing Alkaline Matrix Solubilization. Telmisartan requires a highly alkaline environment to dissolve, while Cilnidipine is light-sensitive. Our bilayer technology ensures each API is released at its peak kinetic window). Cimetidine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Green or Blue). The coating masks the characteristic bitter taste and sulfur-like odor of the drug.
Active Ingredient Strength (Standard) Primary Role Cimetidine USP/BP 200 mg Prophylaxis / Maintenance Cimetidine USP/BP 400 mg Standard Therapeutic Dose Cimetidine USP/BP 800 mg Once-Daily (Bedtime) Excipients Q.S. Povidone / Magnesium Stearate CINITAPRIDE TABLETS
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Dose Gastric Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the hydrogen tartrate salt.
Active Ingredient Strength Primary Clinical Function Cinitapride Hydrogen Tartrate 1 mg The Global Prokinetic Anchor: The definitive therapeutic unit utilized to accelerate gastric emptying and increase esophageal tone in patients with chronic GERD or dyspepsia. Excipients Lactose Monohydrate / Maize Starch / Povidone K-30 / Magnesium Stearate / Hypromellose / Titanium Dioxide (Film Coat) Diluent / Binder / Lubricant / Protective Barrier (Engineered specifically utilizing High-Shear Wet Granulation to ensure 100% uniformity of the microscopic 1mg payload. The premium film coat protects the tablet from atmospheric moisture and masks the bitter taste of the tartrate salt). *Pack Sizes: 10×10 Blisters (Optimized specifically for 15-day to 30-day chronic GI dispensing regimens).
Cinnarizine & Dimenhydrinate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active antihistamine salts.
Active Ingredient Strength Primary Clinical Function Cinnarizine BP/USP 20 mg The Peripheral Stabilizer: Stops the influx of calcium into the inner ear hair cells to dampen the physical sensation of vertigo. Dimenhydrinate BP/USP 40 mg The Central Antiemetic: Blocks H1 and muscarinic receptors in the brain to prevent nausea and motion-induced vomiting. Excipients Microcrystalline Cellulose / Maize Starch / Talc / Magnesium Stearate / Croscarmellose Sodium Diluent / Binder / Glidant / Superdisintegrant (Engineered specifically utilizing High-Shear Dry Blending to ensure 100% uniformity of the active APIs, providing a rapid disintegration profile that delivers relief within 30 minutes of ingestion). *Pack Sizes: 10×10 Blisters (Optimized specifically for short-course acute vertigo regimens).
Ciprofloxacin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is non-negotiable due to the extreme bitterness of the API and its light sensitivity.
Active Ingredient Strength (Standard) Primary Role Ciprofloxacin HCl USP/BP 250 mg Uncomplicated UTI / Mild Infection Ciprofloxacin HCl USP/BP 500 mg Typhoid / Respiratory / Abdominal Ciprofloxacin HCl USP/BP 750 mg Severe / Bone & Joint / Pseudomonas Excipients Q.S. Titanium Dioxide (Opacifier) / Hypromellose Cisplatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution (Liquid) in amber glass vials.
Active Ingredient Strength Concentration Cisplatin USP/BP 10 mg Vial 1 mg/ml (10ml Vol) Cisplatin USP/BP 50 mg Vial 1 mg/ml (50ml Vol) Excipients Sodium Chloride / Mannitol Isotonicity / Diuresis *Pack Sizes: Tray of 1 Vial. (Cytotoxic Packaging).
Citalopram Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the chemical stability of the hydrobromide salt.
Active Ingredient Strength Primary Clinical Function Citalopram Hydrobromide USP/Ph.Eur. 10 mg / 20 mg The Primary Care Anchor: The definitive starting and maintenance doses utilized for the vast majority of patients with moderate depression or panic disorder. Citalopram Hydrobromide USP/Ph.Eur. 40 mg The Severe Refractory Payload: The maximum therapeutic dose utilized for severe depression. (Note: Doses above 40mg are strictly avoided due to cardiac risks). Excipients Lactose Monohydrate / Maize Starch / Croscarmellose Sodium / Magnesium Stearate / Hypromellose / Titanium Dioxide (Film Coat) Diluent / Binder / Superdisintegrant / Lubricant / Opaque Coating (Engineered specifically utilizing High-Shear Wet Granulation to ensure 100% uniformity of the active API, providing a smooth, fast-acting dissolution profile that matches the originator brand). *Pack Sizes: 10×10 Blisters or 28-Tablet Calendar Packs (Optimized for monthly psychiatric compliance).
Citicoline Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Citicoline Sodium USP/BP 500 mg 2 ml Ampoule (250 mg/ml) Citicoline Sodium USP/BP 1000 mg (1 g) 4 ml Ampoule (250 mg/ml) Excipients Water for Injection / pH Adjusters Preservative Free (Single Use) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Citicoline Tablets
FreeProduct Composition & Strength
We supply this product as Controlled Release (CR) Tablets (Film Coated). The matrix formulation is critical to extend the biological half-life.
Active Ingredient Strength Release Profile Primary Indication Citicoline Sodium USP/IP 500 mg Controlled Release Mild Cognitive Impairment / Maintenance Citicoline Sodium USP/IP 1000 mg Controlled Release Acute Stroke Recovery / Severe Dementia Excipients Q.S. HPMC (Release Retardant) / Magnesium Stearate Matrix System Clarithromycin Tablets
FreeClarithromycin Tablets USP 500 mg
Each Filmcoated tablet contains :
Clarithromycin USP 500 mgUsage: – Chest infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Clindamycin & clotrimazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Non-Greasy Vaginal Tablet (V-Tab), packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips, often accompanied by a specialized applicator for sterile insertion.
Active Ingredient Strength Primary Clinical Function Clindamycin Phosphate USP/Ph.Eur. 100 mg The Antibacterial Anchor: The definitive therapeutic unit utilized to eradicate anaerobic bacteria and restore the natural vaginal flora (Lactobacilli). Clotrimazole USP/Ph.Eur. 200 mg The Antifungal Payload: The massive imidazole payload required to penetrate deep into the mucosal layers and destroy recurrent yeast colonies. Excipients Adipic Acid / Sodium Bicarbonate / Lactose / Maize Starch / Magnesium Stearate Effervescent Matrix / Diluent / Disintegrant / Lubricant (Engineered specifically utilizing an Effervescent Vaginal Base. Upon contact with minimal vaginal moisture, the tablet releases microscopic amounts of CO2 to rapidly disperse the active APIs across the entire vaginal vault, ensuring no “untreated zones” remain) *Pack Sizes: 3-Tablet or 7-Tablet Strips (Optimized specifically for the strict, short-course clinical curative regimens).
Clindamycin Capsules
FreeClindamycin capsules are lincosamide antibiotics primarily used to treat serious bacterial infections, including those of the skin, lungs, and internal organs. They are most commonly formulated as Clindamycin Hydrochloride.
Clindamycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Clindamycin Phosphate USP/BP 300 mg 2 ml Ampoule (150 mg/ml) Clindamycin Phosphate USP/BP 600 mg 4 ml Ampoule (150 mg/ml) Excipients Benzyl Alcohol / EDTA Preservative / Stabilizer *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Clindipine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Light-Shielded Cardiovascular Tablet, packed exclusively in highly secure, opaque Alu-Alu blister strips to ensure the absolute chemical stability of the highly photosensitive active ingredient.
Active Ingredient Strength Primary Clinical Function Cilnidipine USP/Ph.Eur. 5 mg The Geriatric & Titration Anchor: The definitive starting dose utilized for elderly patients or those with mild essential hypertension to prevent sudden hypotensive episodes. Cilnidipine USP/Ph.Eur. 10 mg The Global Maintenance Standard: The standardized daily therapeutic payload utilized for the vast majority of adult patients requiring chronic 24-hour blood pressure control. Cilnidipine USP/Ph.Eur. 20 mg The Severe Refractory Macrodose: Utilized strictly for severe, uncontrolled hypertension where the 10mg dose has failed to achieve target blood pressure metrics. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Hypromellose / Magnesium Stearate / Opaque Polymeric Film (Titanium Dioxide base) Diluent / Densifier / Superdisintegrant / Binder / Lubricant / Protective Light Shield (Engineered specifically utilizing a dense, titanium dioxide-heavy film coat. Cilnidipine is intensely sensitive to UV and visible light; this opaque coating guarantees 100% of the active molecule survives to reach the patient’s systemic circulation) *Pack Sizes: 10×10 Opaque Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Clobazam Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The score line is critical for precise titration, especially in pediatric patients.
Active Ingredient Strength (Standard) Primary Role Clobazam USP/BP 5 mg Pediatric Initiation / Titration Clobazam USP/BP 10 mg Standard Maintenance Clobazam USP/BP 20 mg High Dose / Adult Refractory Excipients Q.S. Lactose / Maize Starch / Talc Clofazimine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Micronized Lipid-Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive phenazine dye.
Active Ingredient Strength Primary Clinical Function Clofazimine USP/Ph.Eur. 50 mg The Standard MDT Maintenance Unit: The globally standardized daily dose utilized in the WHO Multi-Drug Therapy (MDT) regimen for Multibacillary Leprosy. Clofazimine USP/Ph.Eur. 100 mg The MDR-TB & Acute ENL Macrodose: The heavy therapeutic payload utilized for the aggressive suppression of acute ENL reactions or as a core component of the standardized short-course MDR-TB regimen. Excipients Microcrystalline Cellulose / Propylene Glycol / Gelatin / Sodium Lauryl Sulfate / Magnesium Stearate / Heavy Opaque Polymeric Film Diluent / Lipid-Solvent Matrix / Binder / Surfactant / Lubricant / Protective Light Shield (Engineered specifically utilizing Advanced API Micronization & Solid-Lipid Tableting. Because Clofazimine is practically insoluble in water, the API is micro-milled and suspended in a specialized surfactant matrix to ensure it absorbs perfectly in the gut without requiring a soft-gelatin encapsulation process) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, continuous, multi-year infectious disease dispensing regimens).
Clomifene citrate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Light-Shielded Fertility Tablet, packed exclusively in highly secure, opaque Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the photosensitive SERM.
Active Ingredient Strength Primary Clinical Function Clomifene Citrate USP/Ph.Eur. 50 mg The Standard Ovulatory Anchor: The definitive starting dose utilized for the first cycle of ovulation induction to assess ovarian response and minimize the risk of dangerous hyperstimulation. Clomifene Citrate USP/Ph.Eur. 100 mg The Refractory Macrodose: The heavy therapeutic payload utilized strictly for subsequent cycles in patients who failed to ovulate (clomifene-resistant PCOS) on the 50mg dose. Excipients Lactose Monohydrate / Maize Starch / Pregelatinized Starch / Magnesium Stearate / Opaque Polymeric Film (Titanium Dioxide base) Diluent / Binder / Disintegrant / Lubricant / Protective Light Shield (Engineered specifically utilizing a dense, titanium dioxide-heavy film coat. Clomifene degrades under direct UV/visible light; this opaque coating guarantees 100% of the active hormone modulator survives from the blister pack to the patient’s stomach) *Pack Sizes: 10-Tablet or 5-Tablet Blisters (Optimized specifically for the strict, 5-day cyclical dosing regimen utilized in reproductive endocrinology).
Clonidine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Small, White). Note: Clonidine is extremely potent and dosed in micrograms (mcg), not milligrams.
Active Ingredient Strength (Metric) Strength (Common) Primary Role Clonidine HCl USP/BP/IP 100 mcg 0.1 mg Initiation / Mild Hypertension Clonidine HCl USP/BP/IP 200 mcg 0.2 mg Standard Maintenance Clonidine HCl USP/BP/IP 300 mcg 0.3 mg High Dose / Crisis Management Excipients Q.S. Lactose / Corn Starch Filler / Binder Clopidogrel & Aspirin Capsules
FreeClopidogrel and Aspirin capsules are a combination of two antiplatelet medications (blood thinners) used primarily to prevent heart attacks and strokes in patients with high cardiovascular risk.
Clopidogrel, Aspirin Tablets Clopidogrel, Aspirin Tablets
FreeA Clopidogrel + Aspirin tablet is a dual antiplatelet therapy (DAPT) used primarily to prevent serious cardiovascular events like heart attacks and strokes
Clotrimazole Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Vaginal Tablets (bullet or almond shaped) with or without an applicator, offering flexible treatment durations.
Active Ingredient Strength Treatment Course Patient Convenience Clotrimazole USP/BP 100 mg 6 Nights Standard Therapy Clotrimazole USP/BP 200 mg 3 Nights Short Course Clotrimazole USP/BP 500 mg 1 Night Single Dose (“One Shot”) Excipients Q.S. Lactose / Adipic Acid / Starch Rapid Disintegration Cloxacillin Capsules
FreeCloxacillin capsules are penicillin-type antibiotics used specifically to treat infections caused by staphylococci (staph infections) that produce an enzyme called penicillinase.
Cloxacillin 1gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cloxacillin Sodium USP/BP Equivalent to 1000 mg (1 g) Cloxacillin Severe Infection / Surgery Sodium Content Approx 2.3 mEq (53 mg) per gram Monitor in Heart Failure *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cloxacillin 500mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cloxacillin Sodium USP/BP Equivalent to 500 mg Cloxacillin Adult Standard Dose Cloxacillin Sodium USP/BP Equivalent to 250 mg Pediatric Dose Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Codeine Phosphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Narcotic Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the alkaloid salt and to strictly prevent diversion.
Active Ingredient Strength Primary Clinical Function Codeine Phosphate USP/Ph.Eur. 15 mg / 30 mg The Standard Analgesic / Antitussive Anchor: The definitive unit utilized for the suppression of severe, dry coughs and the management of mild-to-moderate acute somatic pain. Codeine Phosphate USP/Ph.Eur. 60 mg The Severe Trauma Macrodose: The heavy therapeutic payload utilized strictly for moderate-to-severe refractory pain, often in post-operative or palliative oncology settings. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Densifier / Superdisintegrant / Lubricant / Glidant (Engineered utilizing Strict Geometric Dilution to ensure the opiate payload is flawlessly uniform across every batch, preventing toxic “hot spots” that could trigger accidental respiratory depression) *Pack Sizes: 10×10 Tamper-Evident Blisters (Optimized specifically for strict, closely monitored acute pain dispensing regimens).
Colistimethate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials. Strength is measured in International Units (IU).
Strength (IU) Approximate Mass (mg) Colistin Base Activity (CBA) 1 MIU (1 Million IU) ~80 mg CMS ~34 mg CBA 2 MIU ~160 mg CMS ~68 mg CBA 3 MIU ~240 mg CMS ~100 mg CBA 4.5 MIU ~360 mg CMS ~150 mg CBA Excipients None (Pure Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Collagen Peptide , Sodium Hyaluronate , Chondroitin Sulfate and Vitamin C Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical survival of the intensely sensitive biological payloads.
Active Ingredient Strength Primary Clinical Function Hydrolyzed Collagen Peptides (Type I & II) 150 mg – 500 mg
(Customizable per monograph)The Structural Foundation: The massive, highly bioavailable amino acid payload required to stimulate chondrocyte proliferation and rebuild the physical cartilage matrix. Chondroitin Sulfate Sodium USP/Ph.Eur. 200 mg The Cartilage Hydrator & Shield: Prevents enzymatic cartilage degradation and draws essential water into the articular matrix for compression resistance. Sodium Hyaluronate (Hyaluronic Acid) 30 mg The Synovial Lubricant: Restores the high-viscosity, shock-absorbing properties of the joint capsule fluid. Vitamin C (Ascorbic Acid) USP/Ph.Eur. 35 mg The Biosynthetic Cofactor: The absolute mandatory catalyst required to cross-link the newly formed collagen fibers into a strong, unified matrix. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Glidant / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced Cold-Process High-Shear Granulation. Fluffy collagen peptides are heavily densified without using destructive heat that would instantly oxidize and destroy the Vitamin C payload) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30/60 (Optimized specifically for premium retail presentation and chronic daily compliance).
Corion
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials with a specific solvent.
Active Ingredient Strength (IU) Primary Use Chorionic Gonadotropin USP/BP 5000 IU Standard Ovulation Trigger Chorionic Gonadotropin USP/BP 10000 IU High Dose / IVF Trigger Chorionic Gonadotropin USP/BP 2000 IU Male Hypogonadism / Maintenance Solvent Sodium Chloride (Isotonic) 1 ml or 2 ml Ampoule *Pack Sizes: Tray of 1 Vial + Solvent, 5 Vials + Solvents.
Cyanocobalamin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Standard Use Cyanocobalamin USP/BP 1000 mcg (1 mg) / ml Adult Therapeutic Dose Cyanocobalamin USP/BP 500 mcg / ml Maintenance / Pediatric Excipients Sodium Chloride / Benzyl Alcohol Isotonicity / Preservative *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Cyclophosphamide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cyclophosphamide USP/BP 200 mg Vial Low Dose / Autoimmune Cyclophosphamide USP/BP 500 mg Vial Standard Chemotherapy Cyclophosphamide USP/BP 1000 mg (1 g) Vial High Dose / Hematology Excipients Mannitol / Sodium Chloride Bulking Agent (For Cake Structure) *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Cyclophosphamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Cytotoxic Prodrug Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the sensitive nitrogen mustard derivative and to physically protect caregivers from API exposure.
Active Ingredient Strength Primary Clinical Function Cyclophosphamide USP/Ph.Eur.
(as Cyclophosphamide Monohydrate)50 mg The Oncology & Autoimmune Macrodose: The definitive oral therapeutic unit utilized for chronic, daily continuous “metronomic” chemotherapy regimens and severe immunosuppressive maintenance. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Starch / Magnesium Stearate / Heavy Sucrose or Polymeric Film-Coat Diluent / Densifier / Disintegrant / Lubricant / Protective Cytotoxic Shield (Engineered specifically utilizing a thick, impenetrable sugar or film coat to ensure the highly toxic API never comes into contact with the skin of the patient, pharmacist, or caregiver handling the pill) *Pack Sizes: Bottles of 50/100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic oncology and rheumatology dispensing regimens).
Cyclosporine tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, SMEDDS Liquid-Filled Soft Gelatin Capsule, packed exclusively in highly secure, moisture-resistant heavy-gauge Alu-Alu blister strips to ensure the absolute chemical and physical stability of the volatile microemulsion.
Active Ingredient Strength Primary Clinical Function Cyclosporine USP/Ph.Eur. (Modified) 25 mg / 50 mg The Micro-Titration Anchor: The definitive units utilized for extremely precise, weight-based dose adjustments during the critical early post-transplant phase, or for pediatric dosing. Cyclosporine USP/Ph.Eur. (Modified) 100 mg The Transplant Macrodose: The heavy therapeutic payload required to minimize the total pill burden for adult patients maintaining long-term solid organ graft survival. Excipients (SMEDDS Matrix) Polyoxyl 40 Hydrogenated Castor Oil / Polysorbate 80 / Propylene Glycol / Corn Oil Mono-di-triglycerides / Alpha-Tocopherol Microemulsion Vehicles & Surfactants / Co-Solvent / Lipophilic Carrier / Antioxidant (Engineered specifically to keep the massive lipophilic peptide fully dissolved inside the gelatin shell, instantly forming nanometer-sized droplets upon contact with stomach acid for maximum bioavailability) *Pack Sizes: 5×10 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, lifelong immunosuppressive dispensing regimens).
Cytarabine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution (Liquid) or Lyophilized Powder.
Active Ingredient Strength Format Cytarabine USP/BP 100 mg / 5 ml (20 mg/ml) Ready-to-use Liquid Cytarabine USP/BP 500 mg / 10 ml (50 mg/ml) Ready-to-use Liquid Cytarabine USP/BP 1000 mg (1 g) Vial Lyophilized Powder or Conc. Liquid Excipients Water for Injection Preservative-Free (Available for IT use) *Pack Sizes: Tray of 1 Vial, 5 Vials, or Box of 1/10 Vials.
Dabigatran Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Tartaric Acid-Cored Pellet Formulation, packed exclusively in highly specialized, moisture-blocking Alu-Alu blister strips with integrated desiccants to ensure the absolute chemical survival of the intensely hygroscopic prodrug.
Active Ingredient Strength Primary Clinical Function Dabigatran Etexilate Mesylate USP/Ph.Eur. 75 mg / 110 mg The Renal & Geriatric Anchor: The strictly mandated dose reductions utilized for elderly patients (over 80 years old), patients with moderate renal impairment, or those at an elevated risk of hemorrhagic bleeding. Dabigatran Etexilate Mesylate USP/Ph.Eur. 150 mg The Cardiovascular Macrodose: The massive, globally standardized therapeutic payload required for the aggressive, daily prevention of stroke and systemic embolism in Non-Valvular Atrial Fibrillation (NVAF). Excipients Tartaric Acid (Core) / Hypromellose / Talc / Hydroxypropyl Cellulose / Dimethicone Acidic Microenvironment Generator / Polymer Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced Fluid-Bed Pellet Coating. The tartaric acid core is isolated with a polymer layer, then coated with the Dabigatran API, and sealed again. This prevents the acid from prematurely degrading the drug before it reaches the patient’s stomach) *Pack Sizes: 10×10 Specialized Alu-Alu Blisters or Heavy-Gauge HDPE Bottles with Desiccant Caps (Optimized specifically for absolute moisture defense).
Dacarbazine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in amber glass vials to protect from light.
Active Ingredient Strength Therapeutic Role Dacarbazine USP/BP (DTIC) 200 mg Vial Standard Dose Dacarbazine USP/BP (DTIC) 500 mg Vial High Dose / Multi-use Excipients Citric Acid, Mannitol Stabilizers / pH Adjusters *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Daclatasvir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dihydrochloride Salt Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the active virological agent.
Active Ingredient Strength Primary Clinical Function Daclatasvir Dihydrochloride USP/Ph.Eur. 60 mg The Standard Eradication Macrodose: The definitive, globally standardized daily therapeutic payload utilized for the vast majority of patients to achieve a Sustained Virologic Response (SVR12 – Clinical Cure). Daclatasvir Dihydrochloride USP/Ph.Eur. 30 mg The CYP3A4 Titration Unit: The strict, mandatory dose-reduction unit utilized for patients who are co-infected with HIV and taking strong CYP3A inhibitors (like Ritonavir or Atazanavir). Excipients Anhydrous Lactose / Microcrystalline Cellulose / Croscarmellose Sodium / Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film (Opadry Green) Diluent / Densifier / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced dissolution-enhancing matrices to ensure the Dihydrochloride salt separates perfectly in gastric fluid, guaranteeing maximum systemic bioavailability) *Pack Sizes: Heavy-Gauge HDPE Bottles of 28 (Optimized exactly for a 4-week supply in strict 12-week or 24-week curative regimens).
Dapagliflozin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive propanediol monohydrate active ingredient.
Active Ingredient Strength Primary Clinical Function Dapagliflozin (as Propanediol Monohydrate) USP/Ph.Eur. 5 mg The Titration & Hepatic Anchor: The definitive starting dose utilized for patients with severe hepatic impairment or those at high risk for volume depletion (hypotension). Dapagliflozin (as Propanediol Monohydrate) USP/Ph.Eur. 10 mg The Cardio-Renal Macrodose: The massive, globally standardized therapeutic payload required for the aggressive, daily maintenance of Heart Failure, CKD, and Type 2 Diabetes. Excipients Microcrystalline Cellulose / Anhydrous Lactose / Crospovidone / Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Densifier / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing Strict Low-Humidity Granulation to prevent the highly sensitive API from degrading during compression, sealed with an impenetrable film-coat to block environmental moisture and ensure rapid gastric dissolution) *Pack Sizes: 10×10 Alu-Alu Blisters or 14/28-Tablet Calendar Packs (Optimized specifically for strict chronic cardio-renal dispensing regimens).
Dapsone Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White). The range of strengths allows for precise dosing in both leprosy programs and dermatological maintenance.
Active Ingredient Strength (Standard) Primary Role Dapsone USP/BP 25 mg Pediatric / Initiation Dapsone USP/BP 50 mg Intermediate Dose Dapsone USP/BP 100 mg Standard Adult MDT Dose Excipients Q.S. Magnesium Stearate / Starch Darifenacin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix Prolonged-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute physical stability of the controlled-release polymer.
Active Ingredient Strength Primary Clinical Function Darifenacin Hydrobromide USP/Ph.Eur.
(Equivalent to Darifenacin base)7.5 mg (PR) The Standard Titration & Geriatric Anchor: The definitive, highly efficacious starting and maintenance dose utilized for the vast majority of patients to control OAB symptoms with minimal side effects. Darifenacin Hydrobromide USP/Ph.Eur. 15 mg (PR) The Severe Refractory Macrodose: High-efficacy therapeutic payload utilized strictly for patients who require greater symptom relief and have demonstrated high tolerability to the 7.5 mg dose. Excipients Hypromellose (HPMC) / Dibasic Calcium Phosphate / Magnesium Stearate / Polyethylene Glycol / Titanium Dioxide / Premium Polymeric Film Hydrophilic PR Matrix / Diluent / Lubricant / Plasticizer / Opaque Film (Engineered specifically utilizing high-viscosity Hypromellose. Upon contact with gastrointestinal fluids, the tablet hydrates to form a thick, gelatinous outer layer that strictly controls the diffusion of the highly soluble hydrobromide salt over a 24-hour period) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic urological dispensing regimens).
Daunorubicin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in red-capped glass vials.
Active Ingredient Strength Appearance Daunorubicin Hydrochloride USP/BP Equivalent to 20 mg Daunorubicin Red-Orange Lyophilized Cake Excipients Mannitol Bulking Agent *Pack Sizes: Tray of 1 Vial. (Cytotoxic Packaging).
Deferasirox Tablets
FreeProduct Composition & Strength
We supply this product across two distinct, Precision-Blended Engineering Platforms, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute physical and chemical stability of the active pharmaceutical ingredient.
Active Ingredient Strength & Form Primary Clinical Function Deferasirox USP/Ph.Eur. 125 mg / 250 mg / 500 mg (Dispersible) The Pediatric Suspension Standard: Engineered with micro-crystalline disintegrants to rapidly dissolve in water or apple juice for precise, weight-based pediatric dosing. Deferasirox USP/Ph.Eur. 90 mg / 360 mg (Film-Coated) The High-Compliance Macrodose: The highly densified, lactose-free therapeutic payload designed to be swallowed whole, minimizing GI distress for adult patients. (Note: 360mg FCT is clinically equivalent to 500mg DT). Excipients (FCT Matrix) Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Poloxamer 188 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Solubilizer / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced High-Shear Wet Granulation and Poloxamer Solubilization. Because the FCT tablet is highly densified, it requires elite surfactants to guarantee instantaneous release and absorption in the gastrointestinal tract without the need for pre-dispersion) *Pack Sizes: 10×10 Alu-Alu Blisters or Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for strict, 30-day chronic hematology dispensing regimens).
Deferiprone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, heavy-gauge HDPE bottles to ensure the absolute physical and chemical stability of the massive active pharmaceutical payload.
Active Ingredient Strength Primary Clinical Function Deferiprone USP/Ph.Eur. 500 mg The Standard Titration Unit: The baseline therapeutic dose utilized for precise, weight-based titration in pediatric and lower-weight thalassemia patients. Deferiprone USP/Ph.Eur. 1000 mg The Hematology Macrodose: The massive therapeutic payload required to minimize the total daily pill burden for adult patients suffering from severe, refractory iron overload. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced High-Shear Wet Granulation. Because a 1000mg tablet is inherently massive, it must be highly densified to remain swallowable, heavily coated to mask its severe bitterness, and packed with elite disintegrants to ensure it shatters instantly in the stomach) *Pack Sizes: Heavy-Gauge HDPE Bottles of 50 or 100 (Optimized specifically for massive, multi-pill daily chronic dispensing regimens).
Deflazacort Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Steroidal Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the glucocorticoid prodrug.
Active Ingredient Strength Primary Clinical Function Deflazacort USP/Ph.Eur. 6 mg The Pediatric & Titration Standard: The definitive unit utilized for weight-based dosing in pediatric Duchenne Muscular Dystrophy, slow tapering protocols, and chronic low-dose maintenance for rheumatoid arthritis. Deflazacort USP/Ph.Eur. 30 mg The Acute Flare-Up Macrodose: High-efficacy therapeutic payload utilized for the immediate, aggressive suppression of severe allergic anaphylaxis, acute asthma exacerbations, and violent autoimmune flare-ups. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Binder / Superdisintegrant / Lubricant / Glidant (Engineered utilizing Extreme Multi-Stage Geometric Dilution to ensure the steroidal payload is flawlessly uniform, manufactured under strict OEB 4 containment protocols to prevent cross-contamination and protect facility operators) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict titration, tapering, and chronic immunological dispensing regimens).
Desloratidine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Dissolution Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent API.
Active Ingredient Strength Primary Clinical Function Desloratadine USP/Ph.Eur. 5 mg The Global Allergy & Dermatology Anchor: The definitive once-daily therapeutic unit utilized for the continuous, 24-hour baseline control of Allergic Rhinitis (Hay Fever) and severe Chronic Urticaria. Excipients Microcrystalline Cellulose / Dibasic Calcium Phosphate / Maize Starch / Talc / Premium Polymeric Film Diluent / Densifier / Disintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing elite rapid-burst disintegrants to ensure the tablet shatters instantly in gastric fluid. The dense polymer coating masks the inherent bitterness of the API, ensuring a flawless patient experience) *Pack Sizes: 10×10 Blisters or Bottles of 30 (Optimized specifically for strict, 30-day chronic allergy and dermatology dispensing regimens).
Desmopressin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extreme Microdose Peptide Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical stability of the fragile acetate salt.
Active Ingredient Strength Primary Clinical Function Desmopressin Acetate USP/Ph.Eur.
(Equivalent to Desmopressin base)0.1 mg The Titration & Pediatric Anchor: The definitive starting dose utilized for primary nocturnal enuresis in children or baseline control of Central Diabetes Insipidus. Desmopressin Acetate USP/Ph.Eur. 0.2 mg The Maintenance Macrodose: High-efficacy therapeutic payload utilized for severe, refractory polyuria and nocturia in adults. Excipients Lactose Monohydrate / Potato Starch / Povidone K-30 / Magnesium Stearate Diluent / Disintegrant / Binder / Lubricant (Engineered specifically utilizing Strict Geometric Dilution to ensure the microscopic peptide payload is flawlessly uniform, manufactured under stringent low-moisture conditions to prevent hydrolytic degradation of the fragile peptide bonds) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30/100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic endocrine dispensing regimens).
Desvenlafaxine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix Extended-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical and physical stability of the controlled-release polymer.
Active Ingredient Strength Primary Clinical Function Desvenlafaxine Succinate USP/Ph.Eur.
(Equivalent to Desvenlafaxine base)50 mg (ER) The Global Therapeutic Standard: The definitive, highly efficacious starting and maintenance dose utilized for the vast majority of patients suffering from Major Depressive Disorder. Desvenlafaxine Succinate USP/Ph.Eur. 100 mg (ER) The Severe Refractory Macrodose: High-efficacy therapeutic payload utilized strictly for severe, treatment-resistant depression where maximum norepinephrine reuptake inhibition is required. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Talc / Magnesium Stearate / Premium Polymeric Film Hydrophilic ER Matrix / Diluent / Glidant / Lubricant / Film-Coating (Engineered specifically utilizing high-viscosity Hypromellose. Upon contact with gastric fluid, the tablet forms a thick, gelatinous outer layer that slowly erodes over 24 hours, guaranteeing a smooth, flat pharmacokinetic curve to prevent violent nausea and serotonin spikes) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day psychiatric dispensing regimens).
Dexamethasone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Dexamethasone Sodium Phosphate USP/BP 4 mg (Standard) 1 ml Ampoule (4 mg/ml) Dexamethasone Sodium Phosphate USP/BP 8 mg (High Dose) 2 ml Ampoule (4 mg/ml) Dexamethasone Sodium Phosphate USP/BP 20 mg (Multi-Dose) 5 ml Vial (4 mg/ml) Excipients Creatinine / Sodium Citrate Stabilizers / Buffers *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Dexamethasone Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (typically White, Round, Scored). The scoring allows for precise dose tapering.
Active Ingredient Strength (Standard) Therapeutic Role Dexamethasone USP/BP 0.5 mg Standard Low Dose / Pediatric Dexamethasone USP/BP 4 mg High Dose / Pulse Therapy Dexamethasone USP/BP 8 mg Critical Care / Oncology Excipients Q.S. Lactose / Corn Starch / Magnesium Stearate Diluent / Lubricant Dexlansoprazole & Domperidone Capsules
FreeDexlansoprazole and Domperidone capsules are a combination medication primarily used for erosive esophagitis and Gastroesophageal Reflux Disease (GERD). This combination reduces stomach acid while also speeding up gastric emptying to prevent reflux.
Dexrabeprazole Sodium & Cinitapride Capsules
FreeDexrabeprazole Sodium and Cinitapride capsules are a combination therapy used to treat gastrointestinal disorders such as GERD, peptic ulcers, and delayed gastric emptying. This combination addresses both acid production and gut motility issues.
Dexrabeprazole Sodium & Domperidone Capsules
FreeDexrabeprazole Sodium and Domperidone capsules are combination medications used to treat acid reflux, GERD, and peptic ulcers. They combine a potent acid reducer with a medicine that speeds up stomach emptying.
DI Calcium Phosphate with Vitamin D3 Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (typically White, Round/Oval). The formulation is optimized for disintegration to prevent the “gritty” sensation often associated with phosphate salts.
Active Ingredient Strength (Standard) Therapeutic Role Dibasic Calcium Phosphate IP/USP 500 mg / 1000 mg Source of Calcium & Phosphorus Vitamin D3 (Cholecalciferol) IP/USP 200 IU / 400 IU Absorption Enhancer Excipients Q.S. Maize Starch / Gelatin / Talc Binder / Glidant Diacerein & Glucosamine Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the intensely hygroscopic Glucosamine salt.
Active Ingredient Strength Primary Clinical Function Diacerein USP/Ph.Eur. 50 mg The IL-1β Inhibitor: The potent, slow-acting anti-inflammatory anchor required to halt the enzymatic digestion of joint cartilage. Glucosamine Sulphate Potassium Chloride USP/Ph.Eur.
(Equivalent to Glucosamine Sulphate 750mg)750 mg The Cartilage Substrate: The massive amino-sugar payload required to stimulate proteoglycan synthesis and rebuild the articular matrix. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced Low-Humidity Granulation Technology to process the sticky, highly hygroscopic Glucosamine, sealed with a dense polymer film to block environmental moisture and ensure rapid gastric dissolution of the highly insoluble Diacerein) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, continuous, long-term chronic dispensing regimens).
Diacerein Capsules
FreeDiacerein capsules are a slow-acting treatment primarily used for osteoarthritis of the knee and hip. They work by inhibiting Interleukin-1 (IL-1), a protein that plays a major role in joint inflammation and the destruction of cartilage.
Diazepam Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The score line allows for flexible dosing.
Active Ingredient Strength (Standard) Primary Indication Diazepam USP/BP 2 mg Geriatric / Mild Muscle Spasm Diazepam USP/BP 5 mg Standard Anxiety Dose Diazepam USP/BP 10 mg Severe Spasm / Alcohol Withdrawal Excipients Q.S. Lactose / Maize Starch Diclofenac Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. Sugar coating is traditional to effectively mask the bitter taste of the API.
Active Ingredient Strength (Standard) Primary Indication Diclofenac Potassium USP/BP 25 mg Pediatric (Older) / Mild Pain Diclofenac Potassium USP/BP 50 mg Standard Adult Acute Dose Diclofenac Potassium USP/BP 75 mg Severe Acute Pain (Post-Op) Excipients Q.S. Sucrose (Coating) / Maize Starch Diclofenac Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Reddish-Brown or White). The coating is essential to mask the intensely bitter and metallic taste of the potassium salt.
Active Ingredient Strength (Standard) Therapeutic Role Diclofenac Potassium USP/BP 25 mg Pediatric (Older Children) / Mild Pain Diclofenac Potassium USP/BP 50 mg Standard Acute Adult Dose Excipients Q.S. Maize Starch / Povidone / Sucrose Disintegrant / Coating Agent Diclofenac Sodium & Serratiopeptidase Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Multi-Particulate or Bilayer Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the sensitive biological enzyme.
Active Ingredient Strength Primary Clinical Function Diclofenac Sodium USP/Ph.Eur. 50 mg Potent peripheral NSAID for sustained localized pain and inflammation blockade. Serratiopeptidase IP/Ph.Eur. 10 mg or 15 mg (Enteric-Coated) Proteolytic enzyme engineered to drain localized post-surgical/traumatic edema. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Magnesium Stearate Enteric Coating Polymer for Serratiopeptidase / Diluent / Lubricant *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for 7-to-14 day post-operative or orthopedic recovery regimens).
Diclofenac Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. We offer both the standard 3ml volume and the advanced 1ml (AQ) technology.
Active Ingredient Strength Technology Variant Diclofenac Sodium USP/BP 75 mg / 3 ml Standard (Propylene Glycol Base) Diclofenac Sodium USP/BP 75 mg / 1 ml AQ / Dynapar Generic (Painless, Water Base) Excipients Benzyl Alcohol / Mannitol Preservative / Stabilizer *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Diclofenac Sodium Paracetamol Serratiopeptidase Tablets
FreeA tablet containing Diclofenac Sodium + Paracetamol + Serratiopeptidase is a triple-action medication formulated to provide comprehensive relief from pain, fever, and inflammation. It is widely used for musculoskeletal disorders, post-surgical recovery, and dental pain.
Diclofenac Tablets
FreeProduct Composition & Strength
We supply this product as Enteric Coated (Gastro-Resistant) Tablets or Sustained Release (SR) Tablets.
Active Ingredient Strength (Standard) Formulation Role Diclofenac Sodium USP/BP 25 mg Enteric Coated Pediatric / Mild Pain Diclofenac Sodium USP/BP 50 mg Enteric Coated Standard Acute Dose Diclofenac Sodium USP/BP 75 mg Enteric Coated / SR Intermediate / Injection Switch Diclofenac Sodium USP/BP 100 mg Sustained Release (SR) Once Daily (Chronic Pain) Dicyclomine & Mefenic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Dicyclomine Hydrochloride USP/Ph.Eur. 10 mg The Anticholinergic Anchor: The potent antimuscarinic payload required to rapidly force smooth muscle relaxation and dry up hyper-secretions in the gut. Mefenamic Acid USP/Ph.Eur. 250 mg The Gynecological Analgesic Payload: The dual-action fenamate NSAID required to crush radiating inflammatory pain and block uterine prostaglandin receptors. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Enteric-Like Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing Bi-Layer Compression Technology to physically separate the highly reactive Dicyclomine from the bulky Mefenamic Acid, ensuring rapid, synchronized gastric dissolution without the APIs degrading each other) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute gynecological and GI dispensing regimens).
Dicyclomine HCL Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Dicyclomine Hydrochloride USP/BP 20 mg 2 ml Ampoule (10 mg/ml) Excipients Sodium Chloride / Water for Injection Isotonic Vehicle *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Dicyclomine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (usually small, white or blue). The dosage allows for flexible titration based on the severity of spasms.
Active Ingredient Strength (Standard) Primary Role Dicyclomine HCl USP/BP/IP 10 mg Pediatric / Mild Cramps Dicyclomine HCl USP/BP/IP 20 mg Adult Standard / IBS Therapy Excipients Q.S. Lactose / Magnesium Stearate Didanosine Capsules
FreeDidanosine capsules, often known by the brand name Videx EC, are delayed-release antiretroviral medications used to treat HIV. They are specifically formulated as enteric-coated beadlets within a capsule to prevent the active medicine from being destroyed by stomach acid.
Dienogest Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent steroidal API.
Active Ingredient Strength Primary Clinical Function Dienogest USP/Ph.Eur. 2 mg The Global Endometriosis Standard: The definitive therapeutic micro-dose utilized globally for the continuous, long-term suppression of pelvic pain, dysmenorrhea, and dyspareunia caused by endometriosis. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the 2mg steroidal payload is flawlessly uniform, finished with an opaque film-coat to seal the potent hormone safely away from factory handlers) *Pack Sizes: 14/28-Tablet Calendar Blisters (Optimized specifically for daily, uninterrupted, long-term gynecological dispensing).
Diethyl Carbamazine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White, circular). The formulation is designed for rapid disintegration to support mass dosing campaigns.
Active Ingredient Strength (Standard) Primary Role Diethylcarbamazine Citrate USP/BP/IP 50 mg Pediatric / Titration Diethylcarbamazine Citrate USP/BP/IP 100 mg Standard Adult Unit Diethylcarbamazine Citrate USP/BP/IP 300 mg (Forte) High Dose / TPE Therapy Excipients Q.S. Dibasic Calcium Phosphate / Starch Digoxin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules.
Active Ingredient Strength Concentration Digoxin USP/BP 500 mcg (0.5 mg) 250 mcg/ml (2 ml Ampoule) Excipients Propylene Glycol / Alcohol Solubilizers (Critical for stability) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Digoxin Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). Due to the potency (measured in micrograms), precise titration options are essential.
Active Ingredient Strength (Standard) Target Patient Digoxin USP/BP/IP 0.0625 mg (62.5 mcg) Pediatric / Severe Renal Failure Digoxin USP/BP/IP 0.125 mg (125 mcg) Geriatric / Maintenance Digoxin USP/BP/IP 0.25 mg (250 mcg) Standard Adult Dose Excipients Q.S. Lactose / Maize Starch Diloxanide Furoate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Luminal-Dispersion Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the anti-parasitic ester.
Active Ingredient Strength Primary Clinical Function Diloxanide Furoate USP/Ph.Eur. 500 mg The Global Anti-Parasitic Standard: The definitive therapeutic macrodose utilized globally for the total luminal eradication of amoebic cysts in asymptomatic carriers and post-dysentery patients. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced high-shear granulation and elite superdisintegrants to ensure the massive 500mg tablet shatters and disperses uniformly across the intestinal lining, maximizing physical contact with the embedded cysts) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, 10-day acute parasitology eradication regimens).
Diltiazem Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Immediate Release) or Sustained Release (SR) Tablets (Matrix Technology).
Active Ingredient Strength Formulation Role Diltiazem HCl USP/BP 30 mg Immediate Release Initial Titration / Angina Diltiazem HCl USP/BP 60 mg Immediate Release Standard Maintenance Diltiazem HCl USP/BP 90 mg / 120 mg Sustained Release (SR) Twice Daily Control Excipients Q.S. HPMC (Release Matrix) / Lactose Controlled Diffusion Diphenoxylate & Atropine Sulfate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extreme Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of both the opioid and the anticholinergic alkaloid.
Active Ingredient Strength Primary Clinical Function Diphenoxylate Hydrochloride USP/Ph.Eur. 2.5 mg The Anti-Diarrheal Anchor: The potent mu-opioid agonist required to physically halt hyperactive intestinal peristalsis. Atropine Sulfate USP/Ph.Eur. 0.025 mg (25 mcg) The Abuse Deterrent (Ultra-Microdose): The anticholinergic alkaloid engineered strictly to prevent deliberate opioid overdosage. Excipients Microcrystalline Cellulose / Sucrose / Maize Starch / Magnesium Stearate / Purified Talc Diluent / Binder / Disintegrant / Lubricant / Glidant (Engineered utilizing Extreme Multi-Stage Geometric Dilution to guarantee the microscopic 25 microgram Atropine payload is flawlessly distributed throughout the tablet, preventing lethal anticholinergic “hot spots”) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute gastrointestinal dispensing regimens).
Diphenylhydantoin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dissolution-Optimized Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive sodium salt.
Active Ingredient Strength Primary Clinical Function Diphenylhydantoin (Phenytoin) Sodium USP/Ph.Eur. 100 mg The Global Epilepsy Standard: The definitive therapeutic unit utilized globally for the chronic, daily maintenance and suppression of tonic-clonic and psychomotor seizures. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Povidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant / Lubricant (Engineered specifically utilizing Strict Particle-Size Distribution (PSD) Control. Because the drug is highly insoluble, the API is micro-milled to an exact, mathematically defined micron size to guarantee a highly predictable, extended dissolution profile in the gut, preventing toxic “dose dumping”) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict chronic neurology dispensing regimens and therapeutic drug monitoring protocols).
Disulfiram Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). The tablets are formulated to dissolve rapidly to ensure quick systemic coverage.
Active Ingredient Strength (Standard) Role Disulfiram USP/BP 250 mg Standard Maintenance Disulfiram USP/BP 500 mg Induction Dose Excipients Q.S. Microcrystalline Cellulose / Starch Divalproex Sodium Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the intensely hygroscopic active ingredient.
Active Ingredient Strength Primary Clinical Function Divalproex Sodium USP/Ph.Eur. 250 mg (DR / ER) The Titration & Pediatric Standard: The definitive unit utilized for careful initial dose titration in adult bipolar patients or weight-based dosing for pediatric epilepsy. Divalproex Sodium USP/Ph.Eur. 500 mg (DR / ER) The Neurology Macrodose: Massive therapeutic payload utilized for the aggressive, sustained suppression of chronic complex partial seizures and acute bipolar mania. Excipients (Enteric DR Formulation) Microcrystalline Cellulose / Croscarmellose Sodium / Povidone / Methacrylic Acid Copolymer (Eudragit) / Triethyl Citrate / Titanium Dioxide Diluent / Superdisintegrant / Binder / Enteric Polymer / Plasticizer / Opaque Film (Engineered specifically utilizing advanced fluid-bed enteric coating to completely shield the highly corrosive valproate compound from the stomach, ensuring the pill only dissolves in the alkaline environment of the small intestine to prevent severe gastric bleeding and vomiting) *Pack Sizes: 10×10 Alu-Alu Blisters or Heavy-Gauge HDPE Bottles (Optimized specifically for strict chronic neurology and psychiatry dispensing regimens).
Dolutegravir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Polymorphically Stabilized Microdose Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the Dolutegravir Sodium salt.
Active Ingredient Strength Primary Clinical Function Dolutegravir (as Sodium) USP/Ph.Eur. 50 mg The Global INSTI Anchor: The definitive therapeutic payload required to force immediate, systemic viral suppression and maintain an undetectable viral load. Excipients D-Mannitol / Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Sodium Stearyl Fumarate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing strict low-moisture granulation to prevent the active Dolutegravir Sodium from undergoing polymorphic shifts during compression, guaranteeing absolute pharmacokinetic bioequivalence) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 or 10×10 Alu-Alu Blisters (Optimized specifically for massive NGO distribution and chronic daily dispensing regimens).
Domperidone & Famotidine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Release FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Domperidone Maleate USP/Ph.Eur. 10 mg The Antiemetic/Prokinetic Anchor: The micro-dose peripheral D2 antagonist required to halt nausea and rapidly accelerate gastric emptying. Famotidine USP/Ph.Eur. 20 mg The Acid Suppressor (NDMA-Free): The highly potent, structurally stable H2-receptor antagonist required to crush basal and food-stimulated gastric acid secretion. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced rapid-burst disintegrants to ensure the tablet dissolves instantly in the stomach for fast relief, heavily coated to protect the APIs from environmental degradation) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for high-volume, rapid-turnover acute GI dispensing).
Domperidone & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Domperidone Maleate USP/Ph.Eur. 10 mg The Antiemetic/Prokinetic Anchor: The micro-dose peripheral D2 antagonist required to halt vomiting and rapidly accelerate gastric emptying. Paracetamol (Acetaminophen) USP/Ph.Eur. 500 mg The Central Analgesic Payload: The massive therapeutic payload required to elevate the central pain threshold and crush acute migraine pain. Excipients Microcrystalline Cellulose / Crospovidone / Maize Starch / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the massive 510mg active core shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the bitter taste of the APIs) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid-response outpatient pain management and acute neurology dispensing).
Domperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Release / MD Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability and instantaneous dissolution of the active ingredient.
Active Ingredient Strength Primary Clinical Function Domperidone Maleate USP/Ph.Eur. 10 mg The Global Antiemetic Standard: The definitive rapid-acting unit utilized globally for the immediate suppression of acute nausea and the acceleration of delayed gastric emptying. Excipients (MD Formulation) Microcrystalline Cellulose / Crospovidone / Mannitol / Aspartame / Peppermint Flavor / Magnesium Stearate Diluent / Superdisintegrant / Cooling Agent / Sweetener / Flavoring (Engineered specifically using elite “Rapid-Burst” superdisintegrants to ensure the Mouth Dissolving tablet shatters in saliva within seconds. This is critical because a vomiting patient physically cannot swallow water or a hard pill without instantly throwing it back up) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, short-term gastrointestinal dispensing regimens).
Donepezil Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White for 5mg and Yellow for 10mg). The film coating aids in swallowing and identification.
Active Ingredient Strength (Standard) Role Donepezil HCl USP/BP 5 mg Initial Titration Dose Donepezil HCl USP/BP 10 mg Standard Maintenance Dose Donepezil HCl USP/BP 23 mg High Dose (Sustained Release – Special Order) Excipients Q.S. Lactose Monohydrate / Starch Doripenem Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Doripenem Monohydrate USP/BP Equivalent to 500 mg Doripenem Standard Adult Dose Doripenem Monohydrate USP/BP Equivalent to 250 mg Renal Impairment Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Dothiepin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Heavy-Coated Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure absolute chemical stability and patient safety.
Active Ingredient Strength Primary Clinical Function Dothiepin (Dosulepin) Hydrochloride USP/Ph.Eur. 25 mg The Titration & Geriatric Standard: The definitive low-dose unit utilized for careful initial titration, daytime anxiety management, or for elderly patients highly sensitive to anticholinergic side effects. Dothiepin (Dosulepin) Hydrochloride USP/Ph.Eur. 75 mg The Nighttime Maintenance Macrodose: High-efficacy therapeutic payload utilized strictly at bedtime to induce heavy sleep and drive profound, long-term monoamine receptor down-regulation. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Maize Starch / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opaque Polymeric Film Diluent / Binder / Disintegrant / Glidant / Heavy Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. Dothiepin hydrochloride is profoundly bitter and can cause local oral anesthesia if it dissolves in the mouth; our elite coating guarantees seamless swallowing and zero taste disruption) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, heavily monitored 30-day psychiatric dispensing regimens).
Doxepin Hydrochloride Capsules
FreeDoxepin Hydrochloride capsules are tricyclic antidepressants (TCAs) used to treat depression, anxiety, and sleep disorders (insomnia).
Doxofylline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the xanthine derivative.
Active Ingredient Strength Primary Clinical Function Doxofylline USP/Ph.Eur. 400 mg The Global Pulmonology Standard: The definitive therapeutic macrodose utilized globally for the rapid and sustained reversal of severe bronchoconstriction in adult asthma and COPD patients. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced rapid-burst disintegrants to ensure the massive 400mg tablet dissolves quickly in the stomach, while the heavy film-coat completely masks the intensely bitter taste characteristic of all xanthine alkaloids) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict chronic respiratory dispensing regimens).
Doxycycline 100mg Capsules
FreeDoxycycline 100mg capsules are broad-spectrum tetracycline antibiotics used for bacterial infections, malaria prophylaxis, and severe acne.
Doxycycline Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in amber glass vials.
Active Ingredient Strength Primary Use Doxycycline Hyclate USP/BP Equivalent to 100 mg Doxycycline Standard Adult Dose Excipients Ascorbic Acid / Mannitol Stabilizer / Bulking Agent *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Doxycycline Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets or Dispersible Tablets. The film coating is essential to prevent esophageal irritation.
Active Ingredient Strength (Standard) Primary Role Doxycycline Hyclate USP/BP 100 mg Standard Adult Dose Doxycycline Monohydrate USP/BP 100 mg Esophageal Safety Variant Excipients Q.S. Microcrystalline Cellulose / Titanium Dioxide Doxylamine Succinate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Release Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the succinate salt.
Active Ingredient Strength Primary Clinical Function Doxylamine Succinate USP/Ph.Eur. 25 mg The Global OTC Sleep Standard: The definitive therapeutic unit utilized globally for the immediate induction of sleep in patients suffering from transient or short-term insomnia. Excipients Microcrystalline Cellulose / Dibasic Calcium Phosphate / Sodium Starch Glycolate / Magnesium Stearate / Premium Polymeric Film Diluent / Densifier / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered specifically utilizing a dense, rapid-dissolving polymeric film to completely mask the notoriously bitter, metallic taste of the succinate salt, while guaranteeing the tablet shatters in the stomach within minutes for fast sleep onset) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for high-volume, over-the-counter retail distribution).
Dried Aluminium Hydroxide & Magnesium Trisilicate Tablet
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (Mint or Orange Flavor) to ensure rapid disintegration and palatability.
Active Ingredient Strength (Standard) Role Dried Aluminium Hydroxide Gel IP/BP/USP 250 mg Acid Neutralizer / Constipating Agent Magnesium Trisilicate IP/BP/USP 500 mg Acid Neutralizer / Adsorbent Excipients Q.S. Sweeteners / Flavoring Agents Dried Aluminium Hydroxide Gel, Magnesium Hydroxide & Dimethylpolysiloxane Tablets
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (typically White or Pink, Mint/Orange Flavored). The chewable format is critical for increasing the surface area for acid neutralization and gas dispersion.
Active Ingredient Strength (Standard) Therapeutic Role Dried Aluminium Hydroxide Gel USP/BP 250 mg / 400 mg Sustained Antacid Magnesium Hydroxide USP/BP 250 mg / 400 mg Rapid Antacid Activated Dimethylpolysiloxane (Simethicone) USP/BP 50 mg / 25 mg Antiflatulent (Gas Relief) Excipients Q.S. Mannitol / Sorbitol / Flavor Sweetener / Coolant Dried Aluminium Hydroxide Gel, Magnesium Trisilicate & Peppermint Oil Tablets
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (typically White, Round, Mint-Flavored). The chewable format is essential to increase the surface area for rapid acid neutralization.
Active Ingredient Strength (Standard) Therapeutic Role Dried Aluminium Hydroxide Gel USP/BP 250 mg Antacid / Adsorbent Magnesium Trisilicate USP/BP 500 mg Antacid / Mucosal Protectant Peppermint Oil USP/BP Q.S. (e.g., 2-5 mg) Carminative / Flavor Excipients Q.S. Mannitol / Sucrose / Menthol Sweetener / Coolant Dried Ferrous Sulfate & Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Red or Brown). The coating masks the metallic taste and protects the iron from oxidation.
Active Ingredient Strength (Standard) Therapeutic Role Dried Ferrous Sulfate USP/BP 200 mg (Eq. to 65 mg Elemental Iron) Standard WHO Prophylaxis Dried Ferrous Sulfate USP/BP 335 mg (Eq. to 100 mg Elemental Iron) Therapeutic / Treatment Dose Folic Acid USP/BP 0.4 mg / 0.5 mg / 1.5 mg DNA Synthesis / Neural Tube Protection Excipients Q.S. Maize Starch / Titanium Dioxide / Red Oxide Disintegrant / Colorant Dried Ferrous Sulphate, Elemental Iron, Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Red, Brown, or Maroon). The coating acts as an oxidation barrier.
Active Salt Equivalent Elemental Iron Therapeutic Role Dried Ferrous Sulphate IP/BP 200 mg 65 mg Elemental Iron WHO Standard Prophylaxis Dried Ferrous Sulphate IP/BP 335 mg 100 mg Elemental Iron Therapeutic Anemia Treatment Folic Acid IP/BP 0.4 mg / 0.5 mg / 1.5 mg Neural Tube Protection Excipients Q.S. Cellulose / Titanium Dioxide / Oxide Colors Filler / Colorant Drotaverine & Aceclofenac Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Drotaverine Hydrochloride USP/Ph.Eur. 80 mg The Spasmolytic Anchor (Forte Dose): The massive isoquinoline payload required to rapidly force smooth muscle relaxation in the ureters, biliary tract, and uterus. Aceclofenac USP/Ph.Eur. 100 mg The Anti-Inflammatory Payload: The potent COX-2 preferential NSAID required to crush the radiating inflammatory pain and tissue swelling. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Enteric-Like Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing Bi-Layer Compression Technology to physically separate the two highly reactive APIs, guaranteeing maximum shelf-life and ensuring rapid, simultaneous gastric dissolution without the APIs degrading each other) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, short-term acute emergency dispensing regimens).
Drotaverine & Mefenamic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Drotaverine Hydrochloride USP/Ph.Eur. 80 mg The Spasmolytic Anchor (Forte Dose): The massive isoquinoline payload required to rapidly force smooth muscle relaxation in the uterus, biliary tract, and intestines. Mefenamic Acid USP/Ph.Eur. 250 mg The Gynecological Analgesic Payload: The potent, dual-action fenamate NSAID required to crush radiating inflammatory pain and block uterine prostaglandin receptors. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Enteric-Like Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing Bi-Layer Compression Technology to physically separate the two active APIs, guaranteeing maximum shelf-life and ensuring rapid gastric dissolution without the APIs chemically degrading each other) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute gynecological and emergency dispensing regimens).
Drotaverine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Drotaverine Hydrochloride USP/BP 40 mg 2 ml Ampoule (20 mg/ml) Excipients Sodium Metabisulfite Antioxidant *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Drotaverine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly bitter hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Drotaverine Hydrochloride USP/Ph.Eur. 40 mg The Standard GI/Gynecology Anchor: The definitive therapeutic unit utilized for irritable bowel syndrome (IBS), routine dysmenorrhea, and mild gastrointestinal cramping. Drotaverine Hydrochloride USP/Ph.Eur. 80 mg (Forte) The Acute Colic Macrodose: Massive therapeutic payload utilized for the immediate, aggressive suppression of agonizing renal colic (kidney stones), biliary colic (gallstones), and severe cervical spasms during labor. Excipients Lactose Monohydrate / Maize Starch / Crospovidone / Talc / Magnesium Stearate / Premium Polymeric Film Diluent / Disintegrant / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the tablet shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the intense, bitter taste of the API) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid-response acute ward dispensing and outpatient pain management).
Duloxetine Capsules
FreeDuloxetine capsules are delayed-release (gastro-resistant) medications used to treat depression, anxiety, and chronic pain. Because the medicine can be destroyed by stomach acid, it is formulated as acid-resistant pellets inside a hard gelatin capsule.
Duloxetine Tablets
FreeProduct Composition & Strength
We supply this product as Gastro-Resistant Tablets or Delayed-Release Capsules (containing enteric-coated pellets). Both forms ensure optimal bioavailability.
Active Ingredient Strength (Standard) Primary Role Duloxetine HCl USP/BP 20 mg Geriatric / Initial Dose Duloxetine HCl USP/BP 30 mg Standard Maintenance (Pain/Anxiety) Duloxetine HCl USP/BP 40 mg High Strength (Specific Mkts) Duloxetine HCl USP/BP 60 mg High Strength (Depression/Neuropathy) Dutasteride Capsules
FreeDutasteride capsules are most commonly available as 0.5 mg soft gelatin capsules. They contain the active drug dissolved in a liquid medium to ensure proper absorption
Dydrogesterone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the retro-steroidal API.
Active Ingredient Strength Primary Clinical Function Dydrogesterone USP/Ph.Eur. 10 mg The Global Fertility & Maternal Standard: The definitive therapeutic unit utilized globally for luteal phase support, miscarriage prevention, and chronic endometriosis management. Excipients Lactose Monohydrate / Hypromellose / Maize Starch / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Disintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing high-shear wet granulation to ensure the 10mg steroidal payload is flawlessly uniform, finished with an opaque film-coat to lock the teratogen/hormone safely away from factory handlers) *Pack Sizes: 10×10 Blisters or Calendar Blisters of 14/28 (Optimized specifically for precise tracking during the menstrual cycle and IVF protocols).
Ebastine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Dissolution Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the piperidine derivative API.
Active Ingredient Strength Primary Clinical Function Ebastine USP/Ph.Eur. 10 mg The Standard Allergy Anchor: The definitive once-daily unit utilized for the baseline control of Seasonal and Perennial Allergic Rhinitis (Hay Fever). Ebastine USP/Ph.Eur. 20 mg The Dermatology Macrodose: High-efficacy therapeutic payload utilized strictly for severe, refractory Chronic Idiopathic Urticaria (hives) or intensely severe allergic rhinitis. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered utilizing elite rapid-burst disintegrants to ensure the tablet dissolves instantly in gastric fluid, expediting the hepatic conversion to Carebastine for the fastest possible onset of clinical relief) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, 30-day chronic allergy and dermatology dispensing regimens).
Efavirenz ,Emtricitabine & Tenofovir Disoproxil Fumarate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Mega-Dose FDC Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles to ensure the absolute chemical survival of the moisture-sensitive Tenofovir and light-sensitive Efavirenz.
Active Ingredient Strength Primary Clinical Function Efavirenz USP/Ph.Eur. 600 mg The NNRTI Anchor: The massive, highly lipophilic non-nucleoside payload required to force immediate, systemic viral suppression. Emtricitabine (FTC) USP/Ph.Eur. 200 mg The Cytidine Analogue: Provides profound, long-acting intracellular viral suppression to reinforce the backbone. Tenofovir Disoproxil Fumarate (TDF) USP/Ph.Eur. 300 mg The Nucleotide Backbone: The heavy-hitting chain terminator required to completely halt viral DNA elongation. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Hydroxypropyl Cellulose / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Surfactant / Heavy Film-Coating (Engineered utilizing High-Compression Bi-Layer Technology to fuse 1,100mg of active API into a single, aerodynamically shaped tablet that remains easy for patients to swallow, heavily coated to lock out destructive tropical humidity) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for massive NGO distribution and strict 30-day chronic daily dispensing regimens).
Efavirenz Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the highly lipophilic active ingredient.
Active Ingredient Strength Primary Clinical Function Efavirenz USP/Ph.Eur. 600 mg The Global NNRTI Macrodose: The massive therapeutic payload required to force immediate, systemic viral suppression when combined with a dual-NRTI backbone. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Sodium Lauryl Sulfate / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Surfactant / Binder / Heavy Film-Coating (Engineered specifically utilizing powerful surfactants like Sodium Lauryl Sulfate to drastically increase the solubility of the notoriously lipophilic Efavirenz molecule, ensuring rapid and complete gastrointestinal absorption) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 or 10×10 Alu-Alu Blisters (Optimized specifically for massive NGO distribution and chronic daily dispensing regimens).
Elevat
FreeThe term Elevat most commonly refers to Elevat 20 Capsule, a prescription antidepressant. However, depending on the specific product name (such as “Elevat D”), it may contain entirely different active ingredients like vitamins
Emtricitabine & Tenofovir Disoproxil Fumarate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the moisture-sensitive Tenofovir.
Active Ingredient Strength Primary Clinical Function Emtricitabine (FTC) USP/Ph.Eur. 200 mg The Cytidine Analogue: Provides profound, long-acting intracellular viral suppression with an exceptionally favorable safety profile. Tenofovir Disoproxil Fumarate (TDF) USP/Ph.Eur. 300 mg
(Eq. to 245 mg Tenofovir Disoproxil)The Nucleotide Backbone: The heavy-hitting reverse transcriptase inhibitor required to anchor the ARV regimen and prevent viral breakthrough. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Lactose Monohydrate / Magnesium Stearate / Premium Polymeric Film (Opadry) Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing dry-granulation and heavy film-coating to protect the API from atmospheric moisture, ensuring the massive 500mg active payload remains structurally intact and easily swallowable) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for massive NGO distribution and strict 30-day chronic daily dispensing regimens).
Enalapril Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration). The wide range of strengths allows for the “Start Low, Go Slow” dosing strategy essential for heart failure.
Active Ingredient Strength (Standard) Primary Role Enalapril Maleate USP/BP 2.5 mg Heart Failure Initiation Enalapril Maleate USP/BP 5 mg Hypertension Initiation Enalapril Maleate USP/BP 10 mg Maintenance Dose Enalapril Maleate USP/BP 20 mg High Strength Enoxaparin Injection
FreeEnoxaparin Sodium injection (brand name Lovenox) is a sterile, clear, colourless to pale yellow aqueous solution of a low molecular weight heparin (LMWH). It is primarily used to prevent and treat deep vein thrombosis (DVT) and pulmonary embolism.
Active IngredientStrengthTherapeutic RoleEnoxaparin Sodium USP/BP40 mg / 0.4 mlProphylaxis (DVT Prevention)Enoxaparin Sodium USP/BP60 mg / 0.6 mlTreatment (Weight Adjusted)Enoxaparin Sodium USP/BP80 mg / 0.8 mlTreatment (DVT/PE/ACS)OriginPorcine MucosaViral Safety Certified
Entacavir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the potent antiviral API.
Active Ingredient Strength Primary Clinical Function Entecavir (as Monohydrate) USP/Ph.Eur. 0.5 mg The Global Nucleoside-Naive Standard: The definitive ultra-micro-dose utilized for the daily, lifelong suppression of HBV in patients who have never received prior antiviral therapy. Entecavir (as Monohydrate) USP/Ph.Eur. 1.0 mg The Refractory & Cirrhosis Standard: Double-strength therapeutic payload utilized specifically for patients with Lamivudine-resistant HBV viremia or those suffering from decompensated liver cirrhosis. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the microscopic 0.5mg payload is flawlessly distributed throughout the tablet matrix, preventing toxic “hot spots” or sub-therapeutic failures) *Pack Sizes: 3×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic hepatology dispensing regimens).
Epalrestat Sustained Release Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable SR Matrix Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the intensely photolabile molecule.
Active Ingredient Strength Primary Clinical Function Epalrestat USP/Ph.Eur. 150 mg (SR) The Global Diabetology Standard: The definitive macrodose engineered for 24-hour continuous aldose reductase suppression, dramatically improving patient adherence over standard 50mg TID dosing. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Titanium-Dioxide Film Rate-Controlling Polymer / Diluent / Glidant / Lubricant / UV-Barrier Film (Engineered utilizing elite viscosity-grade HPMC to form a gel-matrix in the gut for sustained drug release, finished with a heavy, opaque film-coat to act as an absolute UV/Light barrier) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic diabetic dispensing regimens).
Ergometrine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets. The coating is critical to protect the active ingredient from oxidation and light.
Active Ingredient Strength (Standard) Primary Role Ergometrine Maleate USP/BP 0.2 mg (200 mcg) PPH Prevention / Subinvolution Ergometrine Maleate USP/BP 0.5 mg (500 mcg) High Potency (Specific Mkts) Excipients Q.S. Tartaric Acid (Stabilizer) Ergotamine & Caffeine ,Paracetamol & Prochlorperazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Quad-API Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive ergot alkaloid and phenothiazine components.
Active Ingredient Strength Primary Clinical Function Ergotamine Tartrate USP/Ph.Eur. 1 mg The Vascular Terminator (Micro-Dose): The foundational ergot alkaloid required to aggressively constrict pulsing cranial arteries. Caffeine Anhydrous USP/Ph.Eur. 100 mg The Absorption Catalyst: Enhances Ergotamine bioavailability and accelerates onset of action. Paracetamol (Acetaminophen) USP/Ph.Eur. 250 mg The Central Analgesic (Macro-Dose): Provides immediate, broad-spectrum relief from accompanying head and neck pain. Prochlorperazine Maleate USP/Ph.Eur. 2.5 mg The Antiemetic Anchor (Ultra-Micro-Dose): Lethally blocks the CTZ to prevent vomiting and ensure full gastrointestinal absorption of the FDC. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant (Engineered utilizing extreme multi-stage geometric dilution to flawlessly blend a microscopic 1mg and 2.5mg payload into a massive 250mg/100mg base, guaranteeing absolute content uniformity and zero toxic ‘hot spots’) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, heavily limited acute neurology dispensing to prevent ergot toxicity).
Erlotinib Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the targeted antineoplastic API.
Active Ingredient Strength Primary Clinical Function Erlotinib (as Hydrochloride) USP/Ph.Eur. 100 mg The Pancreatic Oncology Standard: The definitive daily maintenance dose utilized globally in combination with Gemcitabine for advanced, unresectable, or metastatic pancreatic cancer. Erlotinib (as Hydrochloride) USP/Ph.Eur. 150 mg The Thoracic Oncology Standard: Massive therapeutic payload utilized as a first-line, maintenance, or second-line daily monotherapy for EGFR-mutated Non-Small Cell Lung Cancer. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to maximize dissolution of this highly insoluble compound while locking the potent cytotoxic API safely inside the tablet, completely preventing handler exposure to carcinogenic dust) *Pack Sizes: 3×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Erythromycin Capsules
FreeErythromycin capsules are macrolide antibiotics used to treat various bacterial infections. Because erythromycin base is easily destroyed by stomach acid, these capsules are typically formulated as delayed-release systems containing enteric-coated pellets
Erythromycin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Pink/Red). The coating is essential to mask the intensely bitter taste of the API.
Active Ingredient Strength (Standard) Primary Role Erythromycin Stearate USP/BP
(Equivalent to Erythromycin Base)250 mg Pediatric / Mild Infection Erythromycin Stearate USP/BP
(Equivalent to Erythromycin Base)500 mg Adult Standard Dose Excipients Q.S. Maize Starch / Povidone Erythropoietin Prefilled Syringe Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid in a Prefilled Syringe (PFS) with a fine needle.
Active Ingredient Strength (IU) Patient Profile Recombinant Human Erythropoietin 2000 IU / 0.5 ml Maintenance / Low Weight Recombinant Human Erythropoietin 4000 IU / 0.4 ml Standard Dialysis Dose Recombinant Human Erythropoietin 10000 IU / 1.0 ml Chemotherapy / High Dose Stabilizer Human Albumin / Polysorbate Prevents Protein Aggregation *Pack Sizes: Blister Pack of 1 PFS or Box of 6 PFS.
Escitalopram Oxalate & Clonazepam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Escitalopram (as Oxalate) USP/Ph.Eur. 5 mg / 10 mg The Serotonin Anchor (Macro-Dose): The foundational, highly selective SSRI required to cure the underlying clinical depression and generalized anxiety. Clonazepam USP/Ph.Eur. 0.25 mg / 0.5 mg The Anxiolytic Bridge (Micro-Dose): The highly potent, long-acting benzodiazepine required to suppress acute panic attacks and SSRI-induced activation syndrome. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 0.25mg/0.5mg micro-dose of Clonazepam is flawlessly distributed throughout the Escitalopram matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 2-to-4 week short-term bridging regimens before stepping down to Escitalopram monotherapy).
Esomeprazole & Levosulpiride Capsules
FreeEsomeprazole and Levosulpiride capsules are a combination medication primarily used for gastroesophageal reflux disease (GERD) and peptic ulcers in patients who do not respond to a proton pump inhibitor (PPI) alone.
Esomeprazole Capsule
FreeEsomeprazole capsules primarily contain Esomeprazole Magnesium (as a dihydrate or trihydrate) as the active ingredient. Because esomeprazole is “acid-labile” (broken down by stomach acid), these capsules are formulated as delayed-release or gastro-resistant systems containing enteric-coated pellets.
Esomeprazole Domperidone Capsules
FreeEsomeprazole and Domperidone capsules are combination medications containing two active pharmaceutical ingredients, typically formulated as pellets within a hard gelatin capsule.
Esomeprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Form Esomeprazole Sodium USP/BP Equivalent to 40 mg Esomeprazole White to Off-White Cake Excipients Disodium Edetate / Sodium Hydroxide Chelating Agent / pH Adjuster *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Esomeprazole Tablets
FreeProduct Composition & Strength
We supply this product as Gastro-Resistant (Enteric Coated) Tablets. The drug is acid-labile and must pass through the stomach intact to be absorbed in the intestine.
Active Ingredient Strength (Standard) Role Esomeprazole Magnesium Trihydrate USP/BP 20 mg Maintenance / Mild GERD Esomeprazole Magnesium Trihydrate USP/BP 40 mg Erosive Esophagitis / Zollinger-Ellison Excipients Q.S. Enteric Polymers (Methacrylic Acid) Estramustine Phosphate Capsules
FreeEstramustine phosphate capsules typically contain estramustine phosphate sodium as the active medicinal ingredient, along with several inactive excipients to ensure the drug’s stability and delivery.
Ethambutol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often Gray or White). Coating is essential as the API is hygroscopic and has a bitter taste.
Active Ingredient Strength (Standard) Primary Role Ethambutol HCl USP/BP/IP 200 mg Pediatric / Renal Adjustment Ethambutol HCl USP/BP/IP 400 mg Standard Adult Unit Ethambutol HCl USP/BP/IP 600 mg High Strength (Daily Regimen) Ethambutol HCl USP/BP/IP 800 mg Intensive Phase Loading Ethambutol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential as Ethambutol HCl is highly hygroscopic (absorbs moisture) and has a bitter taste.
Active Ingredient Strength (Standard) Role in DOTS Therapy Ethambutol HCl USP/BP 200 mg Pediatric / Renal Adjustment Ethambutol HCl USP/BP 400 mg Standard Adult Unit Ethambutol HCl USP/BP 600 mg / 800 mg High Weight Band / Forte Ethambutol HCl USP/BP 1000 mg High Dose (Special Order) Excipients Q.S. Sorbitol / Magnesium Stearate Ethamsylate tablets
FreeAn Ethamsylate tablet is a hemostatic (antihemorrhagic) medication used to prevent and control excessive bleeding, particularly from small blood vessels (capillaries).
Ethamsylate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Oxidation-Resistant Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical survival of the highly reactive active ingredient.
Active Ingredient Strength Primary Clinical Function Ethamsylate USP/Ph.Eur. 250 mg The Prophylactic Surgical Standard: Base therapeutic unit utilized for pre-operative dosing to prevent excessive capillary oozing during delicate ENT (tonsillectomy) or dental procedures. Ethamsylate USP/Ph.Eur. 500 mg The Acute Gynecology Macrodose: Massive therapeutic payload utilized for the aggressive, immediate suppression of severe menorrhagia (heavy menstrual bleeding) and acute trauma. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Sodium Metabisulfite / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Antioxidant / Film-Coating (Engineered specifically incorporating powerful antioxidants and a heavy moisture-barrier film to completely shield the API from atmospheric oxygen, preventing the tablet from degrading and turning black/pink on the shelf) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 5-to-10 day acute surgical and gynecological dispensing regimens).
Ethinyestradiol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hazard-Shielded Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the synthetic steroidal API.
Active Ingredient Strength Primary Clinical Function Ethinylestradiol USP/Ph.Eur. 0.05 mg (50 mcg) The Endocrinology Standard: The definitive micro-dose engineered specifically for female hypogonadism, primary ovarian failure, and strictly monitored estrogen replacement. Ethinylestradiol USP/Ph.Eur. 1 mg The Palliative Oncology Macrodose: Massive therapeutic payload utilized strictly for the aggressive hormonal suppression of advanced, inoperable prostate or breast cancer. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. This completely seals the potent steroidal API, ensuring absolute safety for handlers and guaranteeing zero cross-contamination in the facility) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict chronic endocrine and oncology dispensing regimens).
Ethinylestradiol & Levonorgestrel Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant “Calendar Blister” packs to ensure absolute daily patient compliance and chemical stability.
Active Ingredient Strength Primary Clinical Function Ethinylestradiol USP/Ph.Eur. 0.03 mg (30 mcg) The Estrogenic Anchor: The synthetic estrogen required to suppress FSH release and stabilize the uterine lining to prevent irregular breakthrough bleeding. Levonorgestrel USP/Ph.Eur. 0.15 mg (150 mcg) The Progestin Powerhouse: The highly potent, second-generation progestin required to suppress the LH surge and thicken the cervical mucus. Excipients Lactose Monohydrate / Maize Starch / Povidone K-30 / Magnesium Stearate / Premium Sugar/Film Coating Diluent / Disintegrant / High-Shear Binder / Lubricant (Engineered specifically using elite multi-stage geometric dilution to guarantee the microscopic 30 mcg and 150 mcg payloads are flawlessly distributed, preventing lethal hormonal drops that cause contraceptive failure) *Pack Sizes: 21-Day Active Blisters OR 28-Day Calendar Blisters (21 Active Hormonal Tablets + 7 Placebo/Iron Tablets to enforce daily habit-forming compliance).
Ethionamide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Yellow/Orange). Effective coating is mandatory as the drug causes significant gastric irritation and has a metallic taste.
Active Ingredient Strength (Standard) Target Patient Ethionamide USP/BP/IP 250 mg Standard Adult / Pediatric Unit Excipients Q.S. Microcrystalline Cellulose / Hypromellose Etizolam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the ultra-low-dose API.
Active Ingredient Strength Primary Clinical Function Etizolam JP/Ph.Eur. 0.25 mg The Geriatric & Daytime Standard: The definitive ultra-low-dose unit utilized for daytime anxiety suppression without severe sedation, or for highly sensitive elderly patients. Etizolam JP/Ph.Eur. 0.5 mg / 1 mg The Panic & Insomnia Standard: High-efficacy therapeutic payload utilized for the immediate termination of acute panic attacks and the induction of sleep in severe insomnia. Excipients (MD Formulation) Mannitol / Crospovidone / Aspartame / Peppermint Flavor / Magnesium Stearate Diluent / Superdisintegrant / Sweetener / Flavoring (Engineered specifically using elite “Rapid-Burst” superdisintegrants to ensure the tablet shatters and dissolves in saliva within seconds, masking the chemical taste for maximum patient compliance during severe distress) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, short-term psychiatric dispensing regimens).
Etmsylate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules.
Active Ingredient Strength Volume Etamsylate USP/BP 250 mg 2 ml Ampoule (125 mg/ml) – Standard Etamsylate USP/BP 125 mg 2 ml Ampoule – Pediatric Excipients Sodium Metabisulfite Antioxidant *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Etofylline Theophylline Tablets
FreeProduct Composition & Strength
We supply this product as Prolonged Release (PR/Retard) Tablets or standard Film Coated Tablets.
Formulation Variant Etofylline Strength Theophylline Strength Total Potency Role Standard Tablet 77 mg 23 mg 100 mg Acute / Pediatric Retard 150 115 mg 35 mg 150 mg Mild Maintenance Retard 300 231 mg 69 mg 300 mg Adult Standard (BID) Retard 450 346.5 mg 103.5 mg 450 mg High Dose (OD) Etoricoxib Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (distinctively colored by strength). The coating masks the bitter taste and ensures stability.
Active Ingredient Strength (Standard) Color (Typical) Primary Indication Etoricoxib USP/BP 60 mg Green Osteoarthritis / Chronic Pain Etoricoxib USP/BP 90 mg White Rheumatoid Arthritis / Dental Pain Etoricoxib USP/BP 120 mg Pale Green Acute Gout (Short Term) Everolimus Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Antioxidant-Stabilized Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the highly oxidative, potent API.
Active Ingredient Strength Primary Clinical Function Everolimus USP/Ph.Eur. 0.25 mg / 0.5 mg / 0.75 mg Global Transplant Standard: Ultra-micro doses utilized for strict, lifelong immunosuppression following renal or hepatic allografts. Requires extreme content uniformity to maintain the narrow therapeutic blood trough levels (3 to 8 ng/mL). Everolimus USP/Ph.Eur. 5 mg / 10 mg Global Oncology Standard: Massive-dose antineoplastic payload utilized for the aggressive suppression of Renal Cell Carcinoma, Neuroendocrine Tumors (NETs), and HR+/HER2- Breast Cancer. Excipients Butylated Hydroxytoluene (BHT) / Hypromellose / Lactose Anhydrous / Crospovidone / Magnesium Stearate Antioxidant / Binder / Diluent / Superdisintegrant / Lubricant (Engineered specifically utilizing BHT (Butylated Hydroxytoluene) to prevent the rapid oxidative degradation of the Everolimus molecule, guaranteeing maximum clinical shelf-life and potency across harsh climates) *Pack Sizes: 10×10 Alu-Alu Blisters (Transplant) or 3×10 Alu-Alu Blisters (Oncology – 30 Day Supply).
Exemestane Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the potent steroidal antineoplastic agent.
Active Ingredient Strength Primary Clinical Function Exemestane USP/Ph.Eur. 25 mg Global Adult Oncology Standard: The definitive daily maintenance dose required to maintain absolute, continuous destruction of peripheral aromatase enzymes and keep estrogen levels crashed. Excipients Mannitol / Copovidone / Crospovidone / Sodium Starch Glycolate / Magnesium Stearate / Premium Polymeric Film Diluent / High-Shear Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to lock the highly potent, teratogenic steroidal API safely inside the tablet, completely preventing handler and pharmacist exposure to the hazardous dust) *Pack Sizes: 10×10 Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Famotidine & Domperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density Alu-PVC blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Famotidine USP/Ph.Eur. 20 mg Global Clinical Standard: Safe, NDMA-free H2 antagonist for baseline acid suppression. Domperidone Maleate BP/Ph.Eur. 10 mg (Base Equivalent) Peripheral prokinetic and anti-emetic to accelerate gastric emptying and prevent reflux. Excipients Microcrystalline Cellulose / Maize Starch / Crospovidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Lubricant (Engineered for immediate gastric dissolution and synchronized absorption) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-turnover retail OTC and acute gastroenterology dispensing).
Famotidine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Square or Round). The film coating masks the bitter taste and protects the API from moisture.
Active Ingredient Strength (Standard) Role Famotidine USP/BP 20 mg GERD / Heartburn / Maintenance Famotidine USP/BP 40 mg Ulcer Healing / Hypersecretory States Excipients Q.S. Starch (Disintegrant) / Hypromellose Favipiravir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the active pyrazinecarboxamide derivative.
Active Ingredient Strength Primary Clinical Function Favipiravir USP/Ph.Eur. 200 mg The Global Outbreak Standard: Base therapeutic unit utilized for standard, highly flexible titration during acute viral hemorrhagic fevers or novel influenza outbreaks. Favipiravir USP/Ph.Eur. 400 mg / 800 mg The Pill-Burden Reduction Macrodose: Massive therapeutic payload engineered specifically to solve the severe “Day 1 Loading Dose” compliance nightmare (allowing a patient to take two 800mg pills instead of eight 200mg pills). Excipients Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Colloidal Silicon Dioxide / Sodium Stearyl Fumarate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Lubricant (Engineered specifically utilizing advanced high-shear wet granulation to compress massive, bulky API doses into smooth, easily swallowable tablets, finished with a heavy film-coat to lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters or Complete Therapy “Outbreak Kits” (e.g., 34-tablet or 40-tablet regimen boxes).
Ferrous Acorbate & Folic acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Hematinic FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive iron complex.
Active Ingredient Strength Primary Clinical Function Ferrous Ascorbate USP/Ph.Eur.
(Equivalent to Elemental Iron)100 mg The Hemoglobin Anchor: Massive, highly bioavailable elemental iron payload required to rapidly reverse severe maternal anemia without inducing dose-limiting gastric toxicity. Folic Acid (Vitamin B9) USP/Ph.Eur. 1.5 mg The DNA Synthesizer: Critical micro-dose required to drive red blood cell proliferation and guarantee fetal neurodevelopmental safety. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered specifically using a heavy, dark-colored polymeric film-coat to completely mask the violent, metallic taste of the iron and prevent the tablet from rapidly oxidizing on the shelf) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, daily 9-month prenatal dispensing regimens).
Ferrous Folic Tablets
FreeProduct Composition & Strength
We supply this product primarily as Sugar Coated Tablets (Red/Maroon) to mask the metallic taste, or Film Coated Tablets.
Component Strength (Standard) Strength (Therapeutic) Role Dried Ferrous Sulphate 200 mg
(~60-65 mg Elemental Iron)200 mg
(~60-65 mg Elemental Iron)Hemoglobin Synthesis Folic Acid 0.4 mg (400 mcg) 1.5 mg / 5 mg DNA Synthesis / NTD Prevention Color Red / Maroon Red / Brown Identification Ferrous Fumarate with Folic Acid Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential to mask the metallic taste of iron and prevent the oxidation of the ferrous salt during storage.
Active Ingredient Strength (Standard) Therapeutic Role Ferrous Fumarate BP/USP 200 mg / 300 mg Hematinic (Iron Supplement) Folic Acid BP/USP 0.4 mg / 0.5 mg / 1 mg / 5 mg Vitamin B9 (Folates) Excipients Q.S. Povidone / Talc / Magnesium Stearate Stabilizing Core Matrix Ferrous Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. The sugar coating is critical to mask the strong, astringent metallic taste and prevent gastric nausea.
Active Ingredient Strength Elemental Iron Primary Role Dried Ferrous Sulphate USP/BP 200 mg ~ 65 mg Standard Adult Therapy Dried Ferrous Sulphate USP/BP 300 mg ~ 100 mg High Dose Treatment Excipients Q.S. Sucrose (Coating) / Talc Taste Masking Finasteride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hazard-Shielded Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Finasteride USP/Ph.Eur. 1 mg The Global Dermatology Standard: The definitive micro-dose engineered specifically for the lifelong, daily maintenance of Androgenetic Alopecia (Male Pattern Hair Loss). Finasteride USP/Ph.Eur. 5 mg The Global Urology Standard: High-efficacy macro-dose utilized for the aggressive shrinkage of the prostate gland in symptomatic Benign Prostatic Hyperplasia (BPH). Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Docusate Sodium / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Opadry Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. This completely seals the teratogenic API, ensuring absolute safety for female pharmacists and caregivers handling the medication) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for strict, lifelong chronic urology and dermatology dispensing regimens).
Flavoxate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Flavoxate Hydrochloride USP/Ph.Eur. 200 mg The Global Urological Standard: The definitive macrodose therapeutic unit utilized for rapid, acute suppression of agonizing bladder spasms and chronic overactive bladder maintenance. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the massive 200mg tablet shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the bitter taste) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-4 times daily acute dispensing regimens).
Flucloxacillin and Amoxicillin Capsules
FreeFlucloxacillin and amoxicillin combination capsules (often referred to by trade names like Flamox (cosmos-pharm.com) or Amoxam) contain two distinct penicillin-type antibiotics (hra.nhs.uk) that work together to treat a broader range of bacterial infections.
Flucloxacillin Capsules
FreeFlucloxacillin capsules contain flucloxacillin sodium as the active ingredient, along with specific excipients that vary slightly by manufacturer but typically include a lubricant, a glidant, and sodium.
Flucloxacillin Injection
FreeFlucloxacillin injection is a narrow-spectrum penicillin antibiotic used to treat infections caused by staphylococci. It is typically supplied as a white to off-white sterile powder for reconstitution.
Fluconazole & Ivermectin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Fluconazole USP/Ph.Eur. 150 mg The Antifungal Anchor (Macro-Dose): The foundational triazole payload required to systematically eradicate widespread dermatophytes and yeasts. Ivermectin EP/USP 6 mg / 12 mg The Antiparasitic Assassin (Micro-Dose): The highly potent, targeted neurotoxin required to paralyze burrowing mites, lice, and severe helminthic infections. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 6mg micro-dose of Ivermectin is flawlessly distributed throughout the massive Fluconazole matrix, preventing toxic “hot spots”) *Pack Sizes: Single-Dose Blister Packs (1×1 or 1×2) or 10×10 Blisters (Optimized specifically for rapid NGO deployment and “stat” dosing protocols).
Fluconazole Capsules
FreeFluconazole capsules (commonly known by the brand name Diflucan (pfizermedical.com)) contain the active antifungal ingredient fluoxetine hydrochloride along with a powder fill of inactive excipients and a hard gelatin shell.
Fluconazole Tablets
FreeFLUCONAZOLE TABLETS IP 150 MG
Each uncoated tablet contains:
Fluconazole IP 150 mg Excipients q.s.Nuflucon – 200
Fluconazole Tablets IP 200 mg
Each Uncoated Tablet contains :
Fluconazole IP 200 mgUsage: – Prevent and treat a variety of fungal and yeast infections
Category: – Antifungal Drugs
Therapeutic category: – Antifungal
Fludac
FreeFludac is a brand name for capsules manufactured by Cadila Pharmaceuticals Ltd (amazon.in), used primarily as an antidepressant. It belongs to the class of Selective Serotonin Reuptake Inhibitors (SSRIs) (1mg.com).
Flunarazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the dihydrochloride salt.
Active Ingredient Strength Primary Clinical Function Flunarizine (as Dihydrochloride) USP/Ph.Eur. 5 mg The Pediatric & Geriatric Standard: The definitive low-dose unit required for migraine prophylaxis in children or for treating vertigo in elderly patients who are highly sensitive to drug accumulation. Flunarizine (as Dihydrochloride) USP/Ph.Eur. 10 mg The Global Adult Migraine Standard: High-efficacy adult maintenance dose utilized for maximum suppression of chronic, refractory migraine attacks. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant / Lubricant (Engineered utilizing elite low-dose geometric dilution to guarantee that the 5mg or 10mg micro-dose is flawlessly distributed, preventing accidental drug-accumulation spikes) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, heavily monitored 3-to-6 month neurology dispensing regimens).
Fluoxetine Capsules
FreeFluoxetine capsules, commonly known by the brand name Prozac (accessdata.fda.gov), contain the active antidepressant fluoxetine hydrochloride along with several inactive ingredients that vary by manufacturer and dosage strength.
Flupentixol & Melitracen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, light-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly photolabile thioxanthene derivative.
Active Ingredient Strength Primary Clinical Function Flupentixol (as Dihydrochloride) USP/Ph.Eur. 0.5 mg The Anxiolytic Activator (Ultra-Micro-Dose): The foundational presynaptic autoreceptor antagonist required to rapidly resolve apathy, fatigue, and physical tension. Melitracen (as Hydrochloride) USP/Ph.Eur. 10 mg The Mood Elevator (Micro-Dose): The highly tolerable TCA required to lift the baseline depressive neurosis. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Premium Opaque Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / UV-Barrier Film (Engineered utilizing elite multi-stage geometric dilution to guarantee the lethal 0.5mg micro-dose of Flupentixol is flawlessly distributed throughout the matrix, finished with a heavy, opaque coat to prevent UV degradation) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid-response, short-to-medium term psychiatric and general medicine dispensing regimens).
Fluphenazine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules or Vials.
Active Ingredient Strength Type Fluphenazine Decanoate USP/BP 25 mg 1 ml Ampoule / Vial Fluphenazine Decanoate USP/BP 12.5 mg 0.5 ml Ampoule (Starter Dose) Vehicle Sesame Oil Depot Base Preservative Benzyl Alcohol 1.5% v/v (In Vials) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 10 ml Multi-Dose Vial.
Flutamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the antiandrogen API.
Active Ingredient Strength Primary Clinical Function Flutamide USP/Ph.Eur. 250 mg Global Uro-Oncology Standard: The definitive therapeutic unit utilized for chronic, 8-hourly maintenance in Maximum Androgen Blockade (MAB) protocols. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to lock the potent antiandrogen API safely inside the tablet, completely preventing handler and pharmacist exposure to the hazardous hormonal dust) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, high-volume chronic oncology dispensing regimens).
Fluvoxamine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Scored Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the maleate salt.
Active Ingredient Strength Primary Clinical Function Fluvoxamine Maleate USP/Ph.Eur. 50 mg (Scored) Psychiatric Titration Standard: The definitive base unit required for the slow, highly monitored initiation of therapy to prevent severe nausea and activation syndrome in hyper-anxious patients. Fluvoxamine Maleate USP/Ph.Eur. 100 mg (Scored) Global OCD Maintenance Standard: High-efficacy adult maintenance dose. OCD frequently requires massive dosing (up to 300 mg/day), requiring dense, easily swallowable macrodose tablets. Excipients Mannitol / Microcrystalline Cellulose / Pregelatinized Starch / Sodium Stearyl Fumarate / Premium Hypromellose Film Diluent / Binder / Disintegrant / Lubricant / Slipper-Coating (Engineered specifically to compress the active API securely while utilizing a heavy, slick film-coat to completely mask the intensely bitter taste of Fluvoxamine, ensuring long-term patient compliance) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict 3-to-6 month chronic psychiatric dispensing regimens).
Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Yellow/Orange) in standard therapeutic and prophylactic strengths.
Active Ingredient Strength (Standard) Primary Role Folic Acid USP/BP 400 mcg (0.4 mg) Pre-conception / Prophylaxis Folic Acid USP/BP 1 mg High Risk Prophylaxis Folic Acid USP/BP 5 mg Therapeutic / Anemia Treatment Excipients Q.S. Lactose (Filler) / Starch Folic Acid, Niacinamide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Sugar Coated Tablets (typically Yellow or White). The coating protects the photosensitive vitamins from degradation.
Active Ingredient Strength (Standard) Therapeutic Role Folic Acid USP/BP 1.5 mg / 5 mg DNA Repair / Anemia Prevention Niacinamide USP/BP 20 mg / 50 mg / 100 mg Metabolic Support / Skin Barrier Excipients Q.S. Dibasic Calcium Phosphate / Starch Filler / Disintegrant Fortified Procaine Peniciilin Injection with Streptomycin
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Role Procaine Penicillin G 300,000 IU Sustained Release (24 Hours) Benzyl Penicillin Sodium 100,000 IU Rapid Onset (Peak Levels) Streptomycin Sulfate Equivalent to 0.5 g (500 mg) Base Gram-Negative Coverage Total Formulation 400,000 IU + 0.5 g Standard Adult Dose *Pack Sizes: Tray of 50 Vials or 100 Vials.
Fortified Procaine Penicillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Proportion Role Procaine Penicillin G 300,000 IU (75%) Long Acting (Depot) Benzyl Penicillin Sodium 100,000 IU (25%) Rapid Acting (Peak) Total Strength 400,000 IU (4 Lac) Standard Adult Dose Total Strength 4,000,000 IU (40 Lac) High Dose / Veterinary *Pack Sizes: Tray of 50 Vials or 100 Vials.
Frusemide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Light Sensitive). We offer a wide range of strengths, including high-dose variants for renal failure.
Active Ingredient Strength (Standard) Primary Indication Frusemide USP/BP/IP 20 mg Geriatric / Mild Edema Frusemide USP/BP/IP 40 mg Standard Adult Dose Frusemide USP/BP/IP 500 mg Severe Renal Failure (Dialysis Support) Excipients Q.S. Lactose / Starch / Talc Fulvestrant Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Prefilled Syringes (PFS) or Vials. (Note: This is a high-viscosity injection).
Active Ingredient Strength Volume Fulvestrant USP/BP 250 mg 5 ml Prefilled Syringe (50 mg/ml) Fulvestrant USP/BP 250 mg 5 ml Vial (50 mg/ml) Vehicle Castor Oil / Benzyl Alcohol Viscous Oily Base *Pack Sizes: Box of 1 PFS (with safety needles) or Box of 2 PFS (for 500mg dose).
Furazolidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Light-Shielded Tablet, packed exclusively in highly secure, opaque Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical survival of the intensely photolabile (light-sensitive) nitrofuran molecule.
Active Ingredient Strength Primary Clinical Function Furazolidone USP/Ph.Eur. 100 mg Global Outbreak & Dysentery Standard: The definitive therapeutic unit utilized for rapid, massive-dose eradication of intestinal protozoa and severe bacterial enteritis. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Premium Opacifying Film-Coat Diluent / Superdisintegrant / Binder / Lubricant / UV-Barrier Film (Engineered specifically using heavy Titanium Dioxide film-coating to block ultraviolet light, preventing the yellow Furazolidone powder from oxidizing and degrading into a useless brown paste before ingestion) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid NGO deployment and short-course 5-to-7 day dysentery eradication protocols).
Furosemide & Spironolactone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Furosemide USP/Ph.Eur. 20 mg The Loop Diuretic (Fluid Clearance): Rapidly eliminates severe fluid buildup (edema) from the lungs, abdomen, and peripheral tissues. Spironolactone USP/Ph.Eur. 50 mg The Potassium-Sparing Shield: Blocks aldosterone, prevents toxic cardiac fibrosis, and heavily protects the patient against lethal hypokalemia. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Slipper-Coating (Engineered utilizing advanced wet-granulation to ensure both the rapid-acting Furosemide and the slower-acting Spironolactone dissolve at precise, synchronized rates to guarantee the electrolyte-sparing synergy) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict chronic cardiology and hepatology dispensing regimens).
Furosemide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Furosemide USP/BP 20 mg 2 ml Ampoule (10 mg/ml) – Standard Furosemide USP/BP 40 mg / 4 ml 4 ml Ampoule – High Dose Furosemide USP/BP 250 mg / 25 ml 25 ml Vial – Renal Failure Excipients Sodium Hydroxide / NaCl pH Adjuster / Isotonicity *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Gabapentin & Amitriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 300 mg / 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals. Amitriptyline (as Hydrochloride) USP/Ph.Eur. 10 mg The Synaptic Enhancer (Micro-Dose): The highly potent TCA required to amplify descending pain inhibition and restore sleep patterns. Excipients Microcrystalline Cellulose / Crospovidone / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 10mg micro-dose of Amitriptyline is flawlessly distributed throughout the massive Gabapentin matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Gabapentin & Methylcobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable FDC Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the ultra-fragile B12 molecule.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 300 mg / 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals and stop the shooting pain. Methylcobalamin (Mecobalamin) JP/USP 500 mcg / 1500 mcg The Myelin Regenerator (Micro-Dose): The highly potent, biologically active B12 analogue required to stimulate axonal growth and rebuild the damaged myelin sheath. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Titanium-Dioxide Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered utilizing strictly segregated blending or Bilayer technology to prevent the massive Gabapentin dose from degrading the microscopic Methylcobalamin, finished with a heavy, opaque film-coat to act as an absolute UV/Light barrier) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic diabetic and neurology dispensing regimens).
Gabapentin & Nortriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals. Nortriptyline (as Hydrochloride) USP/Ph.Eur. 10 mg The Synaptic Enhancer (Micro-Dose): The highly potent TCA required to amplify descending pain inhibition and restore sleep patterns. Excipients Microcrystalline Cellulose / Crospovidone / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 10mg micro-dose of Nortriptyline is flawlessly distributed throughout the massive 400mg Gabapentin matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Gabapentin Capsules
FreeGabapentin capsules (commonly 100 mg, 300 mg, and 400 mg) contain the active pharmaceutical ingredient gabapentin USP, along with a variety of inactive excipients that aid in the drug’s delivery and stability.
Gabapentine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the heavily compressed active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 600 mg Global Neuropathy Standard: The definitive high-dose unit utilized for the aggressive, long-term maintenance of severe diabetic peripheral neuropathy and postherpetic neuralgia. Gabapentin USP/Ph.Eur. 800 mg Max-Dose Seizure & Refractory Pain Standard: Massive therapeutic payload utilized for high-dose titration (up to 3600 mg/day) in refractory partial-onset seizures and extreme nerve pain. Excipients Copovidone / Crospovidone / Microcrystalline Cellulose / Magnesium Stearate / Premium Polymeric Film High-Shear Binder / Superdisintegrant / Diluent / Slipper-Coating (Engineered specifically utilizing advanced wet-granulation to compress the massive, fluffy 800mg API into a dense, smooth, swallowable tablet, preventing the pill from becoming a dangerous choking hazard for elderly patients) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for chronic, high-volume daily dispensing regimens).
Ganciclovir Capsules
FreeGanciclovir capsules (commonly found in 250 mg and 500 mg strengths) contain the active antiviral drug ganciclovir, a synthetic guanine derivative used to treat and prevent cytomegalovirus (CMV) infections
Ganciclovir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the active pharmaceutical ingredient and protect healthcare handlers from cytotoxic exposure.
Active Ingredient Strength Primary Clinical Function Ganciclovir USP/Ph.Eur. 250 mg Renal Titration Standard: Base therapeutic unit utilized for strict, calculated dose reductions in transplant patients suffering from severe renal impairment (low creatinine clearance). Ganciclovir USP/Ph.Eur. 500 mg Global Maintenance Standard: High-efficacy adult maintenance dose utilized for daily, long-term suppression of CMV retinitis to prevent viral relapse. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically to lock the highly mutagenic and carcinogenic API safely inside the tablet, completely preventing caregiver and pharmacist exposure to toxic airborne dust) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 84 (Optimized specifically for strict, high-volume chronic infectious disease dispensing regimens).
Gefitinib tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the targeted antineoplastic agent.
Active Ingredient Strength Primary Clinical Function Gefitinib USP/Ph.Eur. 250 mg Global Adult Oncology Standard: The definitive, highly precise daily maintenance dose required to maintain constant, paralyzing pressure on the mutated EGFR protein to keep the lung cancer in deep molecular remission. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to maximize the dissolution of this poorly soluble compound while locking the cytotoxic API safely inside the tablet, completely preventing handler and pharmacist exposure to the carcinogenic dust) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Gemcitabine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Gemcitabine Hydrochloride USP/BP Equivalent to 200 mg Gemcitabine Low Dose / Adjustment Gemcitabine Hydrochloride USP/BP Equivalent to 1000 mg (1 g) Standard Adult Dose Gemcitabine Hydrochloride USP/BP Equivalent to 1400 mg (1.4 g) High Dose / Large BSA Excipients Mannitol / Sodium Acetate Bulking Agent / Buffer *Pack Sizes: Tray of 1 Vial. (Cytotoxic Packaging).
Gentamicin Injection
FreeGentamicin injection (brand name Garamycin) is a sterile, clear, colourless to slightly yellow aqueous solution of an aminoglycoside antibiotic. It is used to treat serious gram-negative bacterial infections.
Ginkgo Biloba Extract ,Piracetam & Vinpocetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the combined phyto-synthetic payloads.
Active Ingredient Strength Primary Clinical Function Piracetam USP/Ph.Eur. 400 mg / 800 mg The Nootropic Anchor: Massive synthetic payload required to force neuroplasticity, enhance membrane fluidity, and restore memory function in damaged neural networks. Ginkgo Biloba Extract (Standardized) 60 mg The Microcirculatory Botanical: Standardized extract to prevent capillary clotting and shield the brain from oxidative stress. Vinpocetine USP/Ph.Eur. 5 mg The Cerebral Oxygenator (Micro-Dose): Targeted vasodilation of cerebral arteries to immediately restore oxygen delivery to ischemic tissues. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Polyvinylpyrrolidone (PVP) / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Binder / Slipper-Coating (Engineered specifically to compress the incredibly bulky Piracetam alongside the sticky herbal extract into a single, dense, swallowable pill, heavily coated to lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic 3-to-6 month neurology dispensing regimens).
Ginkgo Biloba Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Pharmaceutical-Grade Botanical Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic herbal extract.
Active Ingredient Strength Primary Clinical Function Standardized Ginkgo Biloba Extract (Leaves) 40 mg The Tinnitus & Vertigo Standard: Base therapeutic unit frequently prescribed three times daily for the management of inner-ear microcirculatory disorders (tinnitus and dizziness). Standardized Ginkgo Biloba Extract (Leaves)
*Strictly Standardized to 24% Ginkgo Flavone Glycosides & 6% Terpene Lactones (EGb 761 Equivalent)80 mg / 120 mg The Cognitive & Vascular Standard: High-efficacy adult macro-doses utilized for the targeted treatment of vascular dementia, Alzheimer’s disease adjunct therapy, and intermittent claudication. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Anhydrous Silica / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Lubricant (Engineered utilizing strictly climate-controlled dry-granulation to prevent the intensely sticky botanical extract from agglomerating, heavily coated to lock out humidity and prevent the characteristic pungent botanical odor) *Pack Sizes: 10×10 Blisters or Bottles of 60 (Optimized specifically for chronic, lifelong neuro-vascular maintenance).
Glibenclamide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The tablet is usually white or pink and scored to allow for precise dose titration.
Active Ingredient Strength (Standard) Role Glibenclamide USP/BP 1.25 mg Geriatric / Renal Impairment Glibenclamide USP/BP 2.5 mg Initial Dose / Mild Diabetes Glibenclamide USP/BP 5 mg Standard Therapeutic Dose Excipients Q.S. Lactose (Diluent) / Maize Starch Glibenclamide, Metformin & Pioglitazone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the three highly reactive APIs.
Active Ingredient Strength Primary Clinical Function Glibenclamide USP/Ph.Eur. 5 mg The Secretagogue (Micro-Dose): Triggers rapid, potent insulin release from the pancreas to control acute post-prandial (after-meal) glucose spikes. Pioglitazone (as Hydrochloride) USP/Ph.Eur. 15 mg The Sensitizer (Micro-Dose): Reverses deep cellular insulin resistance in skeletal muscle and adipose tissue. Metformin Hydrochloride USP/Ph.Eur. 500 mg (IR or ER) The Hepatic Anchor (Macro-Dose): Provides baseline suppression of liver glucose production. Frequently formulated in a sustained-release matrix to minimize severe GI side effects. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Hypromellose / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder (ER Polymer) / Lubricant (Engineered utilizing elite multi-stage geometric dilution to guarantee that the lethal 5mg micro-dose of Glibenclamide is flawlessly and evenly distributed throughout the massive 500mg Metformin matrix) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic diabetic dispensing regimens).
Gliclazide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Immediate Release) or Modified Release (MR) Tablets (Once Daily).
Active Ingredient Strength Formulation Role Gliclazide BP/EP 80 mg Immediate Release Standard Divided Dose Gliclazide BP/EP 30 mg Modified Release (MR) Once Daily (Start) Gliclazide BP/EP 60 mg Modified Release (MR) Once Daily (Maintenance) Excipients Q.S. HPMC (Matrix) / Lactose Release Control Glimepiride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (often color-coded by strength). This allows for precise titration from very low doses.
Active Ingredient Strength (Standard) Color Code (Typical) Role Glimepiride USP/BP/IP 1 mg Pink Initial Dose Glimepiride USP/BP/IP 2 mg Green Titration Step 1 Glimepiride USP/BP/IP 3 mg Yellow Titration Step 2 Glimepiride USP/BP/IP 4 mg Blue Maintenance / High Dose Glipizide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Immediate Release) or Extended Release (XL/SR) Tablets using osmotic pump or matrix technology.
Active Ingredient Strength Formulation Role Glipizide USP/BP 5 mg Immediate Release Standard Initial Dose Glipizide USP/BP 10 mg Immediate Release High Potency Maintenance Glipizide USP/BP 5 mg / 10 mg Extended Release (XL) Once Daily (24hr Control) Excipients Q.S. Lactose / Stearic Acid Binder / Lubricant Glucosamine ,Chondroitin & Diacerein Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Oblong Caplet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic sulfate salts.
Active Ingredient Strength Primary Clinical Function Glucosamine Sulfate Potassium Chloride USP/Ph.Eur. 750 mg The Structural Foundation: Massive therapeutic payload required to stimulate raw cartilage synthesis. Chondroitin Sulfate Sodium USP/Ph.Eur. 200 mg / 250 mg The Hydraulic Restorer: Pulls water into the joint matrix to restore physical shock-absorption and elasticity. Diacerein USP/Ph.Eur. 50 mg The Biochemical Brake: Direct Interleukin-1 (IL-1) inhibition to halt the enzymatic degradation of the joint space. Excipients Microcrystalline Cellulose / Povidone K-30 / Croscarmellose Sodium / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / High-Shear Binder / Superdisintegrant / Lubricant / Slipper-Coating (Engineered specifically to compress over 1000mg of bulky, powdery API into a single, dense, swallowable “caplet” without crumbling, heavily coated to mask the bitter taste and lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic orthopedic dispensing regimens).
Glucosamine Capsule
FreeGlucosamine capsules typically contain one or more forms of glucosamine, an amino sugar essential for building cartilage and joint tissues. These active ingredients are often derived from the shells of shellfish (crabs, shrimp, and lobsters) or produced from vegetarian sources like fermented corn or fungi.
Glucosamine Sulphate Chondroitin Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Large Oval/Caplet shape). The formulation is optimized for high bioavailability and stability.
Active Ingredient Strength Source/Form Glucosamine Sulphate
(as Glucosamine Sulphate Potassium Chloride)500 mg Marine (Shellfish) Exoskeletons Chondroitin Sulphate Sodium 400 mg Bovine / Shark Cartilage (High Purity) Excipients Q.S. PVP K-30 (Binder) / Titanium Dioxide Glyceryl Trinitrate Tablets
FreeProduct Composition & Strength
We supply this product as Sublingual Tablets (Dissolve under tongue) or Sustained Release (SR) Tablets (Swallow whole for prevention).
Active Ingredient Strength Formulation Role Diluted Glyceryl Trinitrate USP 0.5 mg (500 mcg) Sublingual (SL) Acute Attack Rescue Diluted Glyceryl Trinitrate USP 2.6 mg Sustained Release (SR) Angina Prophylaxis Diluted Glyceryl Trinitrate USP 6.4 mg Sustained Release (SR) High Dose Maintenance Excipients Q.S. Lactose (Adsorbent) / Stearates Stability Matrixt Griseofulvin Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). Critical to its efficacy is the particle size; we strictly use Micronized API to ensure adequate absorption.
Active Ingredient Strength (Standard) Form Role Griseofulvin USP/BP 125 mg Micronized Pediatric (Tinea Capitis) Griseofulvin USP/BP 250 mg Micronized Standard Adult Dose Griseofulvin USP/BP 500 mg Micronized High Dose / Resistant Cases Excipients Q.S. Povidone / Maize Starch Binder / Disintegrant Haematinic Capsules
FreeHaematinic capsules are combination supplements containing essential nutrients required for the production of healthy red blood cells and haemoglobin. While specific formulations vary by brand, they typically contain the following categories of ingredients:
Haloperidol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (often small, white or yellow). We offer a wide range of strengths for precise titration.
Active Ingredient Strength (Standard) Primary Role Haloperidol USP/BP 1.5 mg Geriatric / Maintenance Haloperidol USP/BP 5 mg Standard Acute Dose Haloperidol USP/BP 10 mg Severe Psychosis / Mania Haloperidol USP/BP 20 mg Treatment Resistant Cases Heparin Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Vials.
Active Ingredient Strength Volume Heparin Sodium USP/BP 5,000 IU (1,000 IU/ml) 5 ml Multi-Dose Vial Heparin Sodium USP/BP 25,000 IU (5,000 IU/ml) 5 ml Multi-Dose Vial Preservative Benzyl Alcohol 0.95% v/v *Available in preservative-free versions for neonatal use upon request.
HP Kit (Pantoprazole,Metronidazole & Clarithromycin Tablets)
FreeProduct Composition & Strength
We supply this product as a Precision-Packed, Multi-Component Combi-Kit, packed exclusively in highly secure, day-labeled Alu-Alu blister strips to ensure the absolute chemical stability of all three distinct APIs while forcing flawless patient compliance.
Active Component (Per Daily Blister) Strength & Form Primary Clinical Function Pantoprazole Sodium USP/Ph.Eur.
(2 Tablets per kit)40 mg (Gastro-Resistant / Enteric Coated) The Environmental Modulator: Suppresses acid, heals the ulcer, and creates the required pH for antibiotic survival. (Must be heavily enteric-coated to survive the stomach and absorb in the duodenum). Clarithromycin USP/Ph.Eur.
(2 Tablets per kit)500 mg (Film-Coated) The Primary Bacteriostatic: Halts bacterial protein synthesis. Heavy film-coating masks the intensely bitter, metallic macrolide taste. Metronidazole USP/Ph.Eur.
(2 Tablets per kit)400 mg / 500 mg (Film-Coated) The Bactericidal Finisher: Destroys bacterial DNA. Crucial alternative to Amoxicillin for penicillin-allergic demographics or regions with high amoxicillin resistance. *Pack Sizes: 1 Day Kit (containing 6 tablets total: 1 of each for Morning, 1 of each for Evening). Generally supplied in 7-Day or 14-Day Full Therapy Cartons.
Hucog
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection accompanied by a solvent (Sodium Chloride Injection).
Brand Reference Strength Primary Use Hucog / Corion 2000 IU Pediatric Cryptorchidism / Male Fertility Hucog / Corion 5000 IU Standard Ovulation Trigger Hucog / Corion 10000 IU IVF / Assisted Reproductive Technology (ART) Solvent 0.9% NaCl 1 ml or 2 ml Ampoule *Pack Sizes: Single Vial with Ampoule or Tray of 10.
Human Albumin Injection
FreeProduct Composition & Strength
We supply this product as a Ready-to-Use Infusion in glass bottles.
Strength Volume Primary Indication Human Albumin 5% (Iso-oncotic) 250 ml / 500 ml Hypovolemic Shock / Large Burns Human Albumin 20% (Hyper-oncotic) 50 ml / 100 ml Cirrhosis / Ascites / Nephrotic Syndrome Human Albumin 25% (Hyper-oncotic) 50 ml / 100 ml Severe Hypoproteinemia / ICU Support *Stabilizers: Sodium Caprylate and Sodium Acetyltryptophanate (to prevent protein denaturation).
Hydralazine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (often Yellow or Orange). Uncoated tablets are avoided due to stability issues.
Active Ingredient Strength (Standard) Role Hydralazine HCl USP/BP 25 mg Initial Dose / Titration Hydralazine HCl USP/BP 50 mg Maintenance Dose Excipients Q.S. Coating Agents / Stabilizers Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration). Accurate low-dose titration is critical for modern therapy.
Active Ingredient Strength (Standard) Role Hydrochlorothiazide USP/BP 12.5 mg Initial Dose / Combination Use Hydrochlorothiazide USP/BP 25 mg Standard Therapeutic Dose Hydrochlorothiazide USP/BP 50 mg Edema / High Potency Excipients Q.S. Lactose (Filler) / Starch Hydrocortisone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Hydrocortisone Sodium Succinate USP/BP Equivalent to 100 mg Hydrocortisone Standard Adult / Pediatric Emergency Hydrocortisone Sodium Succinate USP/BP Equivalent to 250 mg Severe Asthma / Sepsis Pulse Hydrocortisone Sodium Succinate USP/BP Equivalent to 500 mg High-Dose ICU Protocol Excipients Sodium Phosphate / Sodium Hydroxide Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial + 1 Ampoule (WFI), 10 Vials, or 50 Vials.
Product Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Hydrocortisone Sodium Succinate USP/BP Equivalent to 100 mg Hydrocortisone Standard Adult / Pediatric Emergency Hydrocortisone Sodium Succinate USP/BP Equivalent to 250 mg Severe Asthma / Sepsis Pulse Hydrocortisone Sodium Succinate USP/BP Equivalent to 500 mg High-Dose ICU Protocol Excipients Sodium Phosphate / Sodium Hydroxide Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial + 1 Ampoule (WFI), 10 Vials, or 50 Vials.
Hydrocortisone Oromucosal Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Mucoadhesive Pellet/Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the highly hygroscopic polymers do not prematurely swell from atmospheric humidity.
Active Ingredient Strength Primary Clinical Function Hydrocortisone (as Sodium Succinate or Acetate) USP/Ph.Eur. 2.5 mg Global Oral Pathology Standard: The definitive micro-dose engineered specifically for localized mucosal absorption, maximizing ulcer healing while neutralizing systemic exposure. Excipients Carbomer / Hypromellose (HPMC) / Lactose Monohydrate / Polycarbophil / Magnesium Stearate Bio-Adhesive Polymers / Matrix Former / Diluent / Lubricant (Engineered utilizing elite hydrophilic polymers that instantly cross-link upon contact with saliva, converting the hard tablet into an immovable, slow-release mucosal patch) *Pack Sizes: 10×10 Alu-Alu Blisters or Tubes of 20 (Optimized specifically for the short-term, acute treatment of cyclical ulcer outbreaks).
Hydrocortisone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Scored Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the micronized steroid payload.
Active Ingredient Strength Primary Clinical Function Hydrocortisone USP/Ph.Eur. 5 mg / 10 mg (Scored) Titration & Afternoon Standard: Highly precise, low-dose units engineered for pediatric CAH dosing and the critical “afternoon taper” in adult replacement therapy. Hydrocortisone USP/Ph.Eur. 20 mg (Scored) Morning Surge & Acute Flare Standard: High-efficacy dosing to replicate the natural morning cortisol spike, or for short-term suppression of acute severe allergic or inflammatory conditions. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Magnesium Stearate Diluent / Binder / Superdisintegrant / Lubricant (Engineered utilizing Micronized API—the steroid particles are milled to a microscopic size before blending to guarantee immediate, consistent gastric absorption, which is critical to avoid unpredictable hormone spikes) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict chronic, lifelong endocrinology dispensing regimens).
Hydroxy Chloroquine Sulfate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Heavy-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the photolabile active ingredient.
Active Ingredient Strength Primary Clinical Function Hydroxychloroquine Sulfate USP/Ph.Eur. 200 mg Global Rheumatology Standard: Base therapeutic unit for daily chronic maintenance in SLE and RA, allowing for exact mg/kg dosing based on ideal body weight to prevent toxicity. Excipients Dibasic Calcium Phosphate / Pregelatinized Starch / Magnesium Stearate / Polyethylene Glycol / Premium Titanium Dioxide Opadry Film Diluent / Binder / Lubricant / Heavy Opacifying Film-Coating (Engineered specifically to form an impenetrable light barrier against UV degradation, while completely masking the intensely bitter taste of the sulfate salt to ensure long-term patient compliance) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict 3-to-6 month chronic rheumatology dispensing regimens).
Hydroxyurea Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Scored Film-Coated Tablet, packed exclusively in highly secure, handler-protective Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure absolute chemical stability and prevent accidental cytotoxic exposure.
Active Ingredient Strength Primary Clinical Function Hydroxyurea USP/Ph.Eur. 200 mg / 300 mg / 400 mg Pediatric Sickle Cell Standard: Specialized weight-based units designed for exact mg/kg titration in infants and children suffering from severe vaso-occlusive crises. Hydroxyurea USP/Ph.Eur. 500 mg (Scored) Global Adult Hematology Standard: High-efficacy adult maintenance dose for CML, Polycythemia Vera, and adult Sickle Cell Disease. Excipients Microcrystalline Cellulose / Sodium Citrate / Crospovidone / Magnesium Stearate / Premium Polymeric Film Diluent / pH Stabilizer / Superdisintegrant / Slipper-Coating (Engineered specifically with a heavy, durable film-coat to completely seal the highly toxic, mutagenic core away from nurses, parents, and pharmacists) *Pack Sizes: Bottles of 100 or 10×10 Alu-Alu Blisters (Optimized specifically for massive-volume NGO procurement and chronic lifetime dispensing).
Hyoscine Butylbromide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules.
Active Ingredient Strength Volume Hyoscine Butylbromide USP/BP 20 mg 1 ml Ampoule (Standard Dose) Excipients Sodium Chloride / Water for Injection Isotonic Solution *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 100 Ampoules.
Hyoscine Butylbromide Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets or Film Coated Tablets. The coating is essential to mask the naturally bitter taste of the active ingredient and ensure patient compliance.
Active Ingredient Strength (Standard) Therapeutic Role Hyoscine Butylbromide BP/USP 10 mg Muscarinic Antagonist (Antispasmodic) Excipients Q.S. Calcium Hydrogen Phosphate / Maize Starch Stabilizing Core Matrix Coating Agent Q.S. Sucrose / Talc / Acacia Traditional Sugar Coating Ibuprofen & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating protects the gastric mucosa from direct contact with Ibuprofen and masks the bitter taste of the active ingredients.
Active Ingredient Strength (Standard) Therapeutic Role Ibuprofen BP/USP 200 mg NSAID (Anti-inflammatory/Analgesic) Paracetamol BP/USP 325 mg Analgesic & Antipyretic Excipients Q.S. Starch / Croscarmellose Sodium Disintegrant & Binder Ibuprofen Solution For Infusion
FreeProduct Composition & Strength
We supply this product in two formats: Ready-to-Use Infusion and Concentrate for Dilution.
Active Ingredient Strength Format Ibuprofen (with Arginine) 400 mg / 100 ml Ready-to-Use (IV Bag/Bottle) Ibuprofen (with Arginine) 400 mg / 4 ml Concentrate (Vial – Must Dilute) Solubilizer L-Arginine Ensures Water Solubility *Pack Sizes: 100 ml Bottle (Single) or Tray of 10 Vials.
Ibuprofen Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated (Round/Pink) or Film Coated Tablets. Effective taste-masking is critical as Ibuprofen has a burning aftertaste.
Active Ingredient Strength (Standard) Role Ibuprofen IP/BP/USP 200 mg OTC Standard / Fever Ibuprofen IP/BP/USP 400 mg Prescription Strength / Dental Pain Ibuprofen IP/BP/USP 600 mg Rheumatoid Arthritis (High Dose) Ibuprofen IP/BP/USP 800 mg Severe Osteoarthritis / Acute Injury Imatinib Capsules
FreeImatinib capsules contain the active oncology drug and a specific set of inactive ingredients designed to stabilize the compound for oral delivery.
Imatinib Mesylate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the mesylate salt.
Active Ingredient Strength Primary Clinical Function Imatinib (as Mesylate) USP/Ph.Eur. 100 mg Pediatric & Titration Standard: Base therapeutic unit utilized for weight-based pediatric leukemia dosing, or for highly precise adult dose adjustments during acute hematological toxicity. Imatinib (as Mesylate) USP/Ph.Eur. 400 mg Global Adult Oncology Standard: High-efficacy adult maintenance dose, typically taken once daily for the chronic phase of CML, or twice daily for accelerated phases and GIST. Excipients Microcrystalline Cellulose / Crospovidone / Hypromellose / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Iron-Oxide Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically to lock the cytotoxic API safely inside the tablet, completely preventing handler and pharmacist exposure to the carcinogenic dust) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Imidapril Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for precise titration). The standard strengths are optimized for maintenance therapy.
Active Ingredient Strength (Standard) Role Imidapril HCl 5 mg Initial Dose / Renal Impairment Imidapril HCl 10 mg Standard Maintenance Dose Excipients Q.S. Lactose / Macrogol Imipenem & Cilastatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Buffered Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Role Imipenem USP/BP 500 mg Antibiotic (Carbapenem) Cilastatin Sodium USP/BP Equivalent to 500 mg Cilastatin DHP-I Inhibitor Buffer Sodium Bicarbonate pH Stabilizer *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Imipramine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (often Red or Blue) to effectively mask the intensely bitter and numbing taste of the API.
Active Ingredient Strength (Standard) Primary Role Imipramine HCl USP/BP 25 mg Pediatric Enuresis / Initial Dose Imipramine HCl USP/BP 50 mg Adult Maintenance Imipramine HCl USP/BP 75 mg High Potency (Hospital Use) Excipients Q.S. Sucrose / Talc (Coating) Indapamide Tablets
FreeProduct Composition & Strength
We supply this product as Sugar/Film Coated Tablets (Immediate Release) or Sustained Release (SR) Tablets.
Active Ingredient Strength Formulation Role Indapamide USP/BP 1.5 mg Sustained Release (SR) Modern Standard Dose (24hr Control) Indapamide USP/BP 2.5 mg Immediate Release Classic Maintenance Dose Excipients Q.S. HPMC (Matrix) / Lactose Release Control Indinavir Sulphate Capsules
FreeIndinavir sulphate capsules contain the active antiviral drug and several inactive ingredients used to stabilize the medication for the treatment of HIV-1 infection.
Indomethacin Capsules
FreeIndomethacin capsules contain the active nonsteroidal anti-inflammatory drug (NSAID) and a few standard pharmaceutical fillers to ensure the medication is delivered effectively
Indomethacin Tablets
FreeProduct Composition & Strength
We supply this product as Hard Gelatin Capsules (Standard) or Sustained Release (SR) Tablets.
Active Ingredient Strength (Standard) Form Role Indomethacin USP/BP 25 mg Capsule Standard Adult Dose Indomethacin USP/BP 50 mg Capsule Acute Gout / Severe Pain Indomethacin USP/BP 75 mg SR Capsule / Tablet Once/Twice Daily (Maintenance) Iron Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. Sugar coating is traditional to mask the strong metallic taste of iron.
Iron Salt Salt Strength Elemental Iron Folic Acid Primary Use Dried Ferrous Sulphate 200 mg ~65 mg 0.4 mg / 400 mcg Standard Adult Prophylaxis Dried Ferrous Sulphate 200 mg ~65 mg 1 mg / 5 mg Therapeutic (Pregnancy) Ferrous Fumarate 200 mg ~65 mg 0.4 mg / 1.5 mg Sensitive Stomach / Maternal Ferrous Fumarate 300 mg ~100 mg 5 mg Severe Anemia Treatment Iron Sucrose Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dark Brown Solution in Glass Ampoules.
Active Ingredient Strength Elemental Iron Iron Sucrose Complex USP/BP 100 mg / 5 ml 20 mg/ml Iron Sucrose Complex USP/BP 50 mg / 2.5 ml 20 mg/ml pH Range 10.5 – 11.0 Highly Alkaline (Stable) *Pack Sizes: Tray of 5 Ampoules or 10 Ampoules.
Isoniazid Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Scored). It is often co-administered with Pyridoxine (Vitamin B6) to prevent nerve damage.
Active Ingredient Strength (Standard) Target Patient Isoniazid USP/BP/IP 100 mg Pediatric / Prophylaxis Isoniazid USP/BP/IP 300 mg Standard Adult Dose Excipients Q.S. Binder / Disintegrant Isosorbide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Oral) or Sublingual Tablets (Dissolve under tongue).
Active Ingredient Strength Route / Type Role Isosorbide Dinitrate USP/BP 5 mg Sublingual (SL)/ regular Acute Angina Attack Isosorbide Dinitrate USP/BP 10 mg Oral (Swallow) Angina Prophylaxis Isosorbide Dinitrate USP/BP 20 mg Oral (Swallow) Heart Failure / Maintenance Excipients Q.S. Lactose (Diluent) Safety / Bulk Isoxsuprine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Immediate-Release or Sustained-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Isoxsuprine Hydrochloride USP/Ph.Eur. 10 mg (IR) Acute Titration Standard: Immediate-release base unit used for the rapid initiation of therapy or carefully titrated maintenance in sensitive patients. Isoxsuprine Hydrochloride USP/Ph.Eur. 40 mg (SR) Obstetrics Maintenance Standard: High-efficacy, slow-release matrix designed specifically to provide 12-hour continuous tocolysis, vastly improving maternal compliance and protecting the cardiovascular system. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Lactose Monohydrate / Colloidal Silicon Dioxide / Magnesium Stearate ER Polymer / Diluent / Binder / Glidant / Lubricant (Engineered specifically utilizing premium Hypromellose matrices in the 40mg variant to form a robust hydrogel that slowly erodes in the gastrointestinal tract, ensuring steady-state plasma levels) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict obstetric and chronic vascular dispensing regimens).
Itopride Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Off-White) to mask the bitter taste.
Active Ingredient Strength (Standard) Role Itopride HCl 50 mg Standard Therapeutic Dose Itopride HCl 150 mg (SR) Sustained Release (Once Daily) Excipients Q.S. Lactose (Filler) / HPMC (Binder) Itraconazole Capsules
FreeItraconazole capsules contain a combination of the active antifungal drug and specialized inactive ingredients designed to overcome the medication’s poor solubility in water.
Ivabradine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Ivabradine (as Hydrochloride) USP/Ph.Eur. 5 mg Initiation / Titration Standard: Base therapeutic unit utilized twice daily for the safe initiation of therapy, allowing the cardiologist to monitor resting heart rate before upward titration. Ivabradine (as Hydrochloride) USP/Ph.Eur. 7.5 mg Global Maintenance Standard: High-efficacy adult maintenance dose to strictly maintain the resting heart rate between 50 and 60 beats per minute. Excipients Lactose Monohydrate / Maize Starch / Maltodextrin / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Glidant / Lubricant / Film-Coating (Engineered specifically using precise geometric dilution to ensure the micro-dose API is flawlessly distributed, preventing accidental bradycardia from “hot spots” in a poorly blended generic tablet) *Pack Sizes: 10×10 Blisters or Bottles of 56 (Optimized specifically for strict 28-day chronic cardiology dispensing regimens).
Ivermectin Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The dosage is strictly weight-based.
Active Ingredient Strength (Standard) Role Ivermectin USP/BP/EP 3 mg Pediatric / Low Body Weight Ivermectin USP/BP/EP 6 mg Standard Adult Unit Ivermectin USP/BP/EP 12 mg High Strength (Adult Dose) Excipients Q.S. Microcrystalline Cellulose (Filler) Ketoconazole Tablets
FreeProduct Composition & Available Specifications
We supply Ketoconazole in the internationally recognized 200 mg therapeutic dosage configuration, engineered to optimize plasma saturation kinetics and ensure maximum cellular bioavailability.
Active Ingredient Monograph Calibrated Strength Formulation Matrix Delivery System Primary Clinical Application Ketoconazole USP / BP / IP 200 mg Oral Solid Immediate-Release Uncoated Tablet Systemic Antifungal Care: First-line systemic management of blastomycosis, coccidioidomycosis, histoplasmosis, and severe recalcitrant tinea infections. Excipients Pharma Grade Lactose Monohydrate, Corn Starch, Povidone K-30, Magnesium Stearate The Disintegration Scaffold: Calibrated matrix for high mechanical core stability and rapid wicking in gastric fluids. Ketorolac Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Ketorolac Tromethamine USP/BP 30 mg 1 ml Ampoule (Standard Dose) Ketorolac Tromethamine USP/BP 60 mg 2 ml Ampoule (High Dose) Excipients Alcohol USP / Sodium Chloride Solubilizer / Isotonicity *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Ketorolac Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (White/Round). The standard oral dosage is strictly limited due to potency.
Active Ingredient Strength (Standard) Role Ketorolac Tromethamine USP/BP 10 mg Standard Adult Dose Excipients Q.S. Microcrystalline Cellulose / Lactose L- ornithine-L-aspartate tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical and physical stability of the highly hygroscopic amino acid salt.
Active Ingredient Strength Primary Clinical Function L-Ornithine L-Aspartate (LOLA) 150 mg / 250 mg Hepatology Maintenance Standard: Base therapeutic units for long-term chronic management of severe Non-Alcoholic Fatty Liver Disease (NAFLD), alcoholic hepatitis, and mild hyperammonemia. L-Ornithine L-Aspartate (LOLA) 500 mg Acute Detoxification Standard: High-efficacy adult therapy utilized for immediate ammonia reduction and the step-down management of Hepatic Encephalopathy following hospital discharge. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Film-Coating (Engineered specifically to lock out atmospheric moisture, preventing the heavy 500mg amino acid tablet from swelling, cracking, or prematurely degrading before it reaches the patient’s stomach) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, high-volume chronic hepatology dispensing regimens).
L-Methylfolate Calcium ,Pyridoxal-5-Phosphate & Mecobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the three delicate coenzymes.
Active Ingredient Strength Primary Clinical Function L-Methylfolate Calcium USP/Ph.Eur. 1 mg Active Vitamin B9: Direct methyl-donor for homocysteine remethylation and massive neurotransmitter synthesis. Pyridoxal-5-Phosphate (P5P) USP/Ph.Eur. 0.5 mg Active Vitamin B6: Immediate catalyst for transsulfuration; drastically reduces the risk of paradoxical sensory neuropathy seen with cheap Pyridoxine. Mecobalamin (Methylcobalamin) USP/Ph.Eur. 1500 mcg Active Vitamin B12: Direct peripheral nerve repair, myelin synthesis, and essential co-factor for homocysteine neutralization. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / Heavy UV-Blocking Coating (Engineered specifically to form an impenetrable light barrier, completely preventing the photolabile degradation of the active B12 and folate components) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology and diabetic dispensing regimens).
L-Ornithine-L-Aspartate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Hypertonic Solution in Glass Ampoules. (Must be diluted).
Active Ingredient Strength Concentration L-Ornithine-L-Aspartate 5 g (5000 mg) 500 mg/ml (10 ml Ampoule) Excipients Water for Injection – *Pack Sizes: Tray of 5 Ampoules or 10 Ampoules.
Lactobacillus SporogenesTablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Moisture Matrix Tablet, packed exclusively in highly secure Alu-Alu blister strips or tightly sealed Alu-PVC blisters to prevent premature ambient moisture from triggering spore germination prior to ingestion.
Active Ingredient Strength Primary Clinical Function Lactobacillus sporogenes (Bacillus coagulans) Spores 60 Million Spores (CFU) Global Microbiome Standard: High-density, survival-guaranteed spore count to aggressively recolonize the intestinal lining, halt acute diarrhea, and outcompete opportunistic pathogens following heavy antibiotic therapy. Excipients Microcrystalline Cellulose / Lactose Anhydrous / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Glidant / Lubricant (Engineered specifically utilizing ultra-low moisture excipients during dry-blending to ensure the dormant spores are not accidentally “woken up” and destroyed by water activity on the factory floor) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for massive-volume retail pharmacy and pediatric clinic dispensing).
Lamivudine, Zidovudine & Nevirapine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often White or Off-White). This FDC is designed for patients who have successfully completed the Nevirapine “lead-in” phase.
Active Ingredient Strength (Standard) Class Lamivudine USP/BP 150 mg NRTI (Cytidine Analog) Zidovudine USP/BP 300 mg NRTI (Thymidine Analog) Nevirapine USP/BP 200 mg NNRTI Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Lamotrigine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet or Rapid-Dispersible (DT) Tablet, packed exclusively in highly secure Alu-PVC or Alu-Alu blister strips, frequently customized into highly regulated Titration Starter Kits.
Active Ingredient Strength Primary Clinical Function Lamotrigine USP/Ph.Eur. 25 mg (Starter Kit) The SJS-Prevention Standard: Mandatory base unit for the strict, slow titration schedule required to prevent fatal cutaneous reactions. Often formulated as a Dispersible Tablet (DT) for pediatric epilepsy. Lamotrigine USP/Ph.Eur. 50 mg / 100 mg / 200 mg Global Maintenance Standard: High-efficacy adult maintenance doses for lifelong seizure control and bipolar stabilization. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Sucralose & Flavoring (If DT) / Magnesium Stearate Diluent / Superdisintegrant / Binder / Sweetener (Engineered specifically to either swallow intact or disperse rapidly in a teaspoon of water for children or elderly psychiatric patients suffering from dysphagia) *Pack Sizes: 10×10 Blisters, Bottles of 100, or Dedicated 28-Day Titration Calendar Packs (Optimized specifically to eliminate caregiver dosing errors during the critical initiation phase).
Lansoprazole & Domperidone Capsules
FreeLansoprazole and Domperidone combination capsules contain two active medications used to treat symptoms of acid reflux and slow digestion. They are often formulated as multi-particulate systems (pellets or granules) within a single hard gelatin capsule to ensure stable delivery.
Lansoprazole Capsules
FreeLansoprazole capsules are composed of an active drug and various inactive ingredients (excipients) that ensure the medication is released properly in the body.
Lansoprazole Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, MUPS-Based Dispersible Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the delicate, moisture-sensitive micro-pellets.
Active Ingredient Strength Primary Clinical Function Lansoprazole (as Enteric-Coated Micro-Pellets) USP/Ph.Eur. 15 mg Maintenance & Pediatric Standard: Base therapeutic unit for healing maintenance, pediatric GERD, and preventing NSAID-induced gastric ulcers. Lansoprazole (as Enteric-Coated Micro-Pellets) USP/Ph.Eur. 30 mg Acute Healing Standard: High-efficacy adult dosing for the rapid healing of erosive esophagitis, active duodenal ulcers, and H. pylori eradication protocols. Excipients Methacrylic Acid Copolymer (Enteric Coat) / Crospovidone / Microcrystalline Cellulose / Mannitol / Sucralose / Strawberry Flavor Acid-Resistant Shield / Superdisintegrant / Diluent / Sweetener (Engineered specifically to create a highly palatable, rapid-burst suspension that masks the bitter API, ensuring high pediatric compliance and smooth NG tube transit) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, highly monitored hospital and outpatient dispensing regimens).
Lansoprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Form Lansoprazole Sodium USP/BP Equivalent to 30 mg Lansoprazole White Lyophilized Cake Excipients Mannitol / Meglumine / Sodium Hydroxide Bulking Agent / pH Stabilizer *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Ledipasvir & Sofosbuvir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dual-Active FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles with specialized desiccants to ensure the absolute chemical survival of the complex antiviral APIs.
Active Ingredient Strength Primary Clinical Function Ledipasvir USP/Ph.Eur. 90 mg The NS5A Anchor: Potent inhibitor of viral assembly and secretion; highly effective against specific HCV genotypes. Sofosbuvir USP/Ph.Eur. 400 mg The NS5B Backbone: The globally recognized foundational DAA that forces viral RNA chain termination across multiple genotypes. Excipients Copovidone / Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Binder / Diluent / Superdisintegrant / Lubricant / Film-Coating (Engineered specifically to solve the massive solubility differences between the highly soluble Sofosbuvir and the poorly soluble Ledipasvir, guaranteeing synchronized gastric release and peak systemic absorption) *Pack Sizes: Bottles of 28 (Optimized specifically for the strict 4-week dispensing intervals required for 8, 12, or 24-week curative regimens).
Ledipasvir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Solid-Dispersion Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical survival of the complex antiviral API.
Active Ingredient Strength Primary Clinical Function Ledipasvir USP/Ph.Eur. 90 mg Global Hepatology Standard: The definitive daily dose required to maintain constant, paralyzing pressure on the NS5A viral protein across the entire 12-to-24 week curative cycle. Excipients Copovidone / Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Solubility Enhancer / Diluent / Superdisintegrant / Lubricant / Film-Coating (Engineered specifically utilizing Amorphous Solid Dispersion techniques with Copovidone to force the highly insoluble Ledipasvir to dissolve instantly in gastric fluid, guaranteeing maximum systemic bioavailability) *Pack Sizes: Bottles of 28 or 10×10 Blisters (Optimized specifically for strict 4-week dispensing intervals to match custom DAA combination regimens).
Lenalidomide Capsules
FreeLenalidomide capsules (brand name Revlimid) are a potent immunomodulatory medication used to treat certain types of cancers, such as multiple myeloma and myelodysplastic syndromes.
Letrozole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the micro-dosed endocrine disruptor.
Active Ingredient Strength Primary Clinical Function Letrozole USP/Ph.Eur. 2.5 mg Global Oncology & Fertility Standard: The universal therapeutic unit utilized for 5-to-10 year daily adjuvant breast cancer therapy, or short 5-day cyclic dosing for ovulation induction. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Glidant / Slipper-Coating (Engineered specifically using elite geometric dilution to ensure the microscopic 2.5mg active payload is flawlessly distributed throughout the tablet, guaranteeing absolute content uniformity) *Pack Sizes: 10×10 Blisters or Bottles of 30 (Optimized specifically for strict, heavily monitored chronic oncology dispensing or monthly fertility cycles).
Levetiracetam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Colorless Solution in glass vials.
Active Ingredient Strength Concentration Levetiracetam USP/BP 500 mg 100 mg/ml (in 5 ml Vial) Excipients Sodium Acetate / Glacial Acetic Acid Buffer / pH Adjuster (5.5) *Pack Sizes: Tray of 5 Vials, 10 Vials, or Single Vial packs.
Levocarnitine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Colorless Solution in glass ampoules or vials.
Active Ingredient Strength Concentration Levocarnitine USP/BP 1 Gram (1000 mg) 200 mg/ml (in 5 ml Ampoule) Excipients Water for Injection pH Adjusted (6.0 – 6.5) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or Single Use Vials.
Levonorgestrel Emergency Contraceptive Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Single-Dose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the potent steroid molecule.
Active Ingredient Strength Primary Clinical Function Levonorgestrel USP/Ph.Eur. 1.5 mg Global Emergency Contraceptive Standard: A massive, single-dose payload designed to instantly halt ovulation within the critical 72-hour post-coital window. Excipients Lactose Monohydrate / Maize Starch / Povidone K30 / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered specifically utilizing advanced micronized API to ensure ultra-rapid gastric dissolution, guaranteeing the hormone hits the bloodstream fast enough to beat the LH surge) *Pack Sizes: 1-Tablet Blister Packs (Optimized specifically for discrete, over-the-counter (OTC) retail and single-dispense NGO crisis kits).
Levosulpiride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the benzamide derivative.
Active Ingredient Strength Primary Clinical Function Levosulpiride USP/Ph.Eur. 25 mg Global Gastroenterology Standard: Base therapeutic unit taken prior to meals for the rapid relief of functional dyspepsia, bloating, and mild gastroparesis. Levosulpiride USP/Ph.Eur. 50 mg / 75 mg Psychiatric & Severe Dysmotility Standard: High-efficacy adult therapy used for severe, treatment-resistant diabetic gastroparesis or utilized by psychiatrists for somatoform disorders and mild depression. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Binder / Glidant (Engineered specifically without heavy polymeric retardants to guarantee immediate, complete gastric dissolution within 10 to 15 minutes of ingestion, preparing the stomach for the incoming meal) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, meal-dependent acute and chronic dispensing regimens).
Lidocaine 2% Ampoules
FreeProduct Composition & Strength
We supply this product as a Sterile, Preservative-Free Solution in glass ampoules.
Active Ingredient Strength Total Content (2ml) Lidocaine Hydrochloride USP/BP 2% (20 mg/ml) 40 mg Total Content (5ml) 2% (20 mg/ml) 100 mg Excipients Sodium Chloride / Water for Injection Isotonic Solution *Available in 2ml, 5ml, and 10ml Type I Glass Ampoules.
Lidocaine Cartridges
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Type I Glass Cartridges.
Active Ingredients Strength Cartridge Volume Lidocaine Hydrochloride 2% (20 mg/ml) 1.8 ml / 2.2 ml Adrenaline (Epinephrine) 1:80,000 / 1:100,000 – Stabilizer Sodium Metabisulfite Antioxidant *Pack Sizes: Box of 50 or 100 Cartridges (Blister packed for sterility).
Lidocaine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Multi-dose Vials.
Active Ingredient Strength Common Application Lidocaine Hydrochloride 1% (10 mg/ml) Infiltration / Minor Suturing / Diagnostic Blocks Lidocaine Hydrochloride 2% (20 mg/ml) Major Nerve Blocks / Epidural / Anti-arrhythmic Excipients Sodium Chloride / Methylparaben (in vials) Isotonicity / Preservative *Available in preservative-free (PF) versions for spinal/epidural use.
Lignocaine Adrenaline Dental Cartridges
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Cartridges with siliconized plungers.
Active Ingredients Strength Standard Cartridge Volume Lignocaine Hydrochloride 2% (20 mg/ml) 1.8 ml (Standard) Adrenaline (Epinephrine) 1:80,000 / 1:100,000 2.2 ml (Extended) Excipients Sodium Metabisulfite / NaCl Antioxidant / Isotonicity *Pack Sizes: Box of 50 Cartridges or 100 Cartridges (Blister packed).
Lignocaine Injection
FreeLignocaine injection (also known as Lidocaine) is a sterile, aqueous solution primarily used as a local anaesthetic and antiarrhythmic agent. Its composition varies depending on whether it is a single-dose or multi-dose formulation and whether it includes a vasoconstrictor.
Linagliptin & Metformin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the highly hygroscopic combination.
Active Ingredient Strength Primary Clinical Function Linagliptin / Metformin HCl (IR) 2.5 mg / 500 mg
2.5 mg / 850 mg
2.5 mg / 1000 mgTwice-Daily Standard: Immediate-release units designed to be taken twice a day with meals to provide rapid, meal-time incretin spikes alongside baseline hepatic suppression. Linagliptin / Metformin HCl (ER) 5 mg / 1000 mg (ER) Once-Daily Premium Standard: High-efficacy Extended-Release therapy designed for ultimate patient compliance, delivering the full daily dose of Linagliptin while slowly trickling Metformin into the gut over 24 hours to prevent severe gastrointestinal side effects. Excipients Hypromellose (HPMC) / Copovidone / Microcrystalline Cellulose / Magnesium Stearate / Premium Moisture-Barrier Film ER Polymer / Binder / Diluent / Lubricant (Engineered utilizing elite Bilayer Rotary Presses to physically separate the delicate 2.5mg/5mg Linagliptin dose from the massive, moisture-drawing Metformin layer, preventing cross-degradation) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 60 (Optimized specifically for strict, massive-volume chronic diabetic dispensing regimens).
Linagliptin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Shielded Film-Coated Tablet, packed exclusively in highly secure Alu-Alu blister strips to ensure the absolute chemical stability of the delicate API.
Active Ingredient Strength Primary Clinical Function Linagliptin USP/Ph.Eur. 5 mg The Universal Standard: A single, high-efficacy maintenance dose that applies to all adult patients, regardless of age, hepatic function, or severe renal impairment. Excipients Mannitol / Pregelatinized Starch / Copovidone / Magnesium Stearate / Premium Opadry Film Diluent / Disintegrant / Binder / Moisture-Barrier Coating (Engineered specifically without highly hygroscopic components to prevent moisture absorption, ensuring rapid disintegration and maximum bioavailability of the 5mg payload) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, massive-volume chronic diabetic dispensing regimens).
Lincomycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Lincomycin Hydrochloride USP/BP 600 mg 2 ml Ampoule (300 mg/ml) – Standard Lincomycin Hydrochloride USP/BP 300 mg 1 ml Ampoule (300 mg/ml) – Pediatric Preservative Benzyl Alcohol 0.945% v/v *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Linezolide Tablets
FreeLinezolide Tablets
Each Film Coated Tablet Contains
Linezolide 600 mgUsage: – Treat different types of bacterial infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotics
Lithium Carbonate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the controlled-release polymers.
Active Ingredient Strength Primary Clinical Function Lithium Carbonate USP/Ph.Eur. 300 mg (IR) Acute Mania Standard: Immediate-release base unit used for the rapid, aggressive titration of serum lithium levels during an active, severe manic episode. Lithium Carbonate USP/Ph.Eur. 400 mg / 450 mg (ER/SR) Global Maintenance Standard: Extended-release therapy designed to flatten the pharmacokinetic curve, preventing toxic blood spikes and minimizing severe hand tremors and nausea during lifelong maintenance therapy. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Sodium Starch Glycolate / Magnesium Stearate / Premium Opadry Film Hydrophilic ER Polymer / Diluent / Disintegrant / Lubricant (Engineered specifically using high-shear wet granulation to form a highly reliable, slow-eroding matrix that trickles the elemental lithium into the bloodstream over 12 hours) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict, massive-volume lifelong psychiatric dispensing regimens).
Liv 52 tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Standardized Herbal Matrix Tablet, packed exclusively in highly secure, moisture-resistant PVC/PVDC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly oxidative botanical alkaloids.
Standardized Botanical Extract Target Biomarker Primary Clinical Function Milk Thistle Ext. (Silybum marianum) Standardized to 70% Silymarin (140 mg) The Antioxidant Anchor: Massive glutathione restoration and hepatocyte membrane stabilization. Andrographis paniculata (Kalmegh) Ext. Standardized to 10% Andrographolides The Choleretic Catalyst: Potent antiviral properties (Hepatitis) and violent stimulation of bile flow to flush out hepatic toxins. Phyllanthus niruri (Bhumyamalaki) Ext. Standardized Bitters The Viral Blocker: Clinically documented to suppress the replication of the Hepatitis B virus and protect against drug-induced liver injury (DILI). Boerhavia diffusa (Punarnava) Ext. Standardized Alkaloids The Hepatic Diuretic: Reduces liver enlargement (hepatomegaly) and flushes out excess fluid accumulation (ascites) caused by liver failure. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Film-Coating (Engineered specifically to lock out atmospheric moisture—which destroys botanical extracts—and completely mask the intensely bitter taste of Kalmegh and Silymarin) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict 3-to-6 month chronic hepatology dispensing regimens).
Loperamide Capsules
FreeLoperamide capsules (most commonly known by the brand name Imodium) are an anti-diarrheal medication used to slow down an overactive bowel. They contain a specific active salt and various inactive ingredients that form the capsule and stabilize the medicine
Lopinavir & Ritonavir Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically Yellow, Oval). The proprietary matrix ensures high bioavailability of poorly soluble Lopinavir.
Active Ingredient Strength (Standard) Therapeutic Role Lopinavir USP/BP 200 mg HIV-1 Protease Inhibitor Ritonavir USP/BP 50 mg Pharmacokinetic Booster (Pediatric Variant) 100 mg Lopinavir + 25 mg Ritonavir Pediatric HIV Management Excipients Q.S. Copovidone / Sorbitan Monolaurate / Silica Solubility Enhancers Losartan Potassium Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically Yellow or White, Oval). The coating protects the hygroscopic Losartan from moisture.
Active Ingredient Strength (Standard) Therapeutic Role Losartan Potassium USP/BP 50 mg Vasodilator (ARB) Hydrochlorothiazide USP/BP 12.5 mg Diuretic (Thiazide) (High Strength Variant) 100 mg Losartan + 25 mg HCTZ Severe Hypertension Excipients Q.S. Microcrystalline Cellulose / Lactose / Magnesium Stearate Filler / Lubricant Losartan Potassium, Amlodipine Besylate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Yellow, Oval/Round). The formulation uses the Besylate salt of Amlodipine for maximum stability.
Active Ingredient Strength (Standard) Therapeutic Role Losartan Potassium USP/BP 50 mg Vasodilator (ARB) Amlodipine Besylate USP/BP 5 mg (Eq. to Base) Vasodilator (CCB) (High Strength Variant) 50 mg Losartan + 10 mg Amlodipine
100 mg Losartan + 5 mg AmlodipineResistant Hypertension Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Filler / Super-Disintegrant Magnesium Sulphate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Hypertonic Solution in Glass Ampoules.
Active Ingredient Concentration Strength (per 2ml) Magnesium Sulphate BP/USP 50% w/v (Standard) 1 Gram (in 2 ml) Magnesium Sulphate BP/USP 25% w/v 0.5 Gram (in 2 ml) Magnesium Sulphate BP/USP 10% w/v 2 Grams (in 20 ml) Osmolarity Approx. 4060 mOsmol/L Highly Hypertonic *Pack Sizes: Tray of 10 Ampoules, 25 Ampoules, or 100 Ampoules.
Maxgalin
FreeMaxgalin is a brand of medication manufactured by Sun Pharmaceutical Industries Ltd., primarily used to treat neuropathic (nerve) pain, fibromyalgia, and certain types of seizures.
Medroxyprogesterone Acetate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Micronized Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the delicate steroid molecule.
Active Ingredient Strength Primary Clinical Function Medroxyprogesterone Acetate USP/Ph.Eur. 2.5 mg / 5 mg HRT Maintenance Standard: Continuous or sequential low-dose therapy for the prevention of endometrial hyperplasia in postmenopausal women receiving estrogen. Medroxyprogesterone Acetate USP/Ph.Eur. 10 mg Acute Gynecology Standard: High-efficacy adult dosing for the rapid arrest of abnormal uterine bleeding and the induction of withdrawal bleeding in secondary amenorrhea. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Lubricant (Engineered specifically utilizing advanced micronized API to overcome the severe hydrophobicity of the steroid, ensuring maximum, predictable gastric absorption) *Pack Sizes: 10×10 Blisters or 14-Day Calendar Packs (Optimized specifically for strict cyclic or continuous gynecological dispensing regimens).
Medroxyprogesterone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Aqueous Suspension in glass vials or prefilled syringes.
Active Ingredient Strength Volume Medroxyprogesterone Acetate USP/BP 150 mg 1 ml Vial (Standard Contraceptive) Medroxyprogesterone Acetate USP/BP 500 mg / 1000 mg High-Dose (Oncology Use) Excipients Polyethylene Glycol / Polysorbate 80 Suspending Agents *Pack Sizes: Single Vial with Syringe, or Tray of 25/50 Vials for Tenders.
Mefanamic Acid & Dicyclomine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant PVC/PVDC or Alu-Alu blister strips to ensure the absolute chemical stability of the combined APIs.
Active Ingredient Strength Primary Clinical Function Mefenamic Acid USP/Ph.Eur. 250 mg The Anti-Inflammatory Anchor: Rapidly reduces prostaglandin-induced pain, uterine inflammation, and heavy menstrual bleeding. Dicyclomine Hydrochloride USP/Ph.Eur. 10 mg The Antispasmodic Catalyst: Instantly relaxes violently contracting smooth muscle in the gastrointestinal and biliary tracts, and the uterus. Excipients Microcrystalline Cellulose / Maize Starch / Sodium Starch Glycolate / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant (Engineered specifically to ensure the bulky Mefenamic Acid powder shatters and dissolves instantly upon reaching the gastric fluid, ensuring the 30-minute rapid onset required for acute pain rescue) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-volume, over-the-counter (OTC) or acute prescription dispensing regimens).
Melphalan Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, handler-protective Amber Glass Bottles or specialized Alu-Alu cold-chain blisters to ensure the absolute chemical survival of the highly unstable alkylating agent.
Active Ingredient Strength Primary Clinical Function Melphalan USP/Ph.Eur. 2 mg Global Oncology Standard: Base therapeutic unit allowing for highly precise, weight-based or Body Surface Area (BSA) calculated “pulsed” dosing regimens. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Glidant / Slipper-Coating (Engineered specifically with a heavy film-coat to ensure immediate gastric transit and to completely seal the highly toxic, mutagenic core away from nurses and caregivers) *Pack Sizes: Amber Glass Bottles of 25/50 Tablets (Optimized specifically for strict, highly monitored hematology dispensing regimens).
Memantine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips, frequently customized into 4-week Titration Starter Packs.
Active Ingredient Strength Primary Clinical Function Memantine (as Hydrochloride) USP/Ph.Eur. 5 mg Initiation / Titration Standard: Base therapeutic unit utilized exclusively for the mandatory 4-week step-up protocol to build patient tolerance and prevent severe CNS adverse effects. Memantine (as Hydrochloride) USP/Ph.Eur. 10 mg Global Neurology Standard: High-efficacy adult maintenance dose, typically taken twice daily, for the sustained neuroprotection of the degenerating brain. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Slipper-Coating (Engineered specifically with a heavy, smooth film-coat to ensure immediate gastric transit and absolute ease of swallowing for elderly patients suffering from severe dysphagia) *Pack Sizes: 10×10 Blisters, Bottles of 60, or Customized 28-Day Titration Starter Kits (Optimized specifically for strict chronic geriatric dispensing regimens).
Mercaptopurine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, handler-protective Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the antimetabolite and protect healthcare workers from cytotoxic exposure.
Active Ingredient Strength Primary Clinical Function Mercaptopurine (as Monohydrate) USP/Ph.Eur. 50 mg Global Oncology & Autoimmune Standard: Scored tablets allowing for highly precise, weight-based or Body Surface Area (BSA) based dose titrations in pediatric and adult populations. Excipients Lactose Monohydrate / Maize Starch / Pregelatinized Starch / Magnesium Stearate / Stearic Acid Diluent / Binder / Disintegrant / Lubricant (Engineered specifically using high-containment wet granulation to prevent airborne cytotoxic dust generation during manufacturing, ensuring precise, even API distribution) *Pack Sizes: Bottles of 25/50 or 10×10 Blisters (Optimized specifically for strict, heavily monitored chronic oncology dispensing regimens).
Meropenem & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Role Meropenem USP/BP 1000 mg (1 g) Broad-Spectrum Carbapenem Sulbactam Sodium USP/BP Equivalent to 500 mg Beta-Lactamase Inhibitor Total Strength 1.5 g (1500 mg) Per Single Dose Vial *Pack Sizes: Single Vial with or without Sterile Water for Injection.
Meropenem Injection
FreeMeropenem injection (brand name Keppra) is a broad-spectrum carbapenem antibiotic supplied as a sterile white to pale yellow powder for reconstitution. It is used to treat severe bacterial infections
Mesalazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, pH-Targeted PR Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly oxidative 5-ASA molecule.
Active Ingredient Strength Primary Clinical Function Mesalazine (5-ASA) USP/Ph.Eur. 400 mg (PR) Initiation / Titration Standard: Base therapeutic unit for mild presentations or pediatric titration in pediatric gastroenterology. Mesalazine (5-ASA) USP/Ph.Eur. 800 mg / 1200 mg (PR) Global Gastroenterology Standard: High-efficacy adult maintenance doses designed to improve patient compliance by drastically reducing the daily pill burden. Excipients Methacrylic Acid Copolymer Type B & C (Eudragit L/S) / Hypromellose / Triethyl Citrate / Iron Oxide Colors / Talc Enteric & Prolonged-Release Polymers / Plasticizer / Glidant (Engineered specifically to form an impenetrable, acid-resistant shield that strictly delays drug release until reaching the high-pH environment of the lower gastrointestinal tract) Metformin Hydrochloride & Glimepiride Tablets
FreeProduct Composition & Strength
We supply this product in Bilayer Tablets or Matrix Tablets packed in Alu-Alu or PVC/PVDC Blisters.
Product Strength Metformin HCl (SR) Glimepiride Common Name 500/1 mg 500 mg 1 mg G1 Tablet 500/2 mg 500 mg 2 mg G2 Tablet 1000/2 mg 1000 mg 2 mg Forte / DS Tablet 1000/4 mg 1000 mg 4 mg High Strength Metformin Hydrochloride & Pioglitazone Tablets
FreeProduct Composition & Strength
We supply this product as Sustained Release (SR) Matrix Tablets packed in Alu-Alu Blisters.
Product Strength Metformin HCl (SR) Pioglitazone Common Name 500/15 mg 500 mg 15 mg Pio-M 15 500/30 mg 500 mg 30 mg Pio-M 30 1000/15 mg 1000 mg 15 mg Pio-M Forte 1000/30 mg 1000 mg 30 mg Pio-M DS Methimazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the thionamide compound.
Active Ingredient Strength Primary Clinical Function Methimazole (Thiamazole) USP/Ph.Eur. 5 mg Maintenance / Titration Standard: Base therapeutic unit for precisely lowering doses as the patient approaches the euthyroid (normal) state, preventing drug-induced hypothyroidism. Methimazole (Thiamazole) USP/Ph.Eur. 10 mg Initial Suppression Standard: High-efficacy adult therapy for rapidly crashing toxic thyroid hormone levels during severe, active hyperthyroidism. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Odor-Masking Coating (Engineered specifically using strict geometric dilution to ensure the microscopic API dose is flawlessly distributed, and fi lm-coated to mask the compound’s inherent sulfurous taste) Methotrexate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Isotonic Solution (Ready-to-Use) or Lyophilized Powder (High Dose).
Active Ingredient Strength Common Application Methotrexate USP/BP 2.5 mg / ml Low Dose (Rheumatology/Dermatology) Methotrexate USP/BP 25 mg / ml Standard Oncology Dose Methotrexate USP/BP 50 mg / 500 mg / 1 g High Dose MTX (Leukemia Protocols) Preservative Benzyl Alcohol Present in Multi-dose Vials (Avoid in IT use) *Pack Sizes: 2 ml Vial, 20 ml Vial, or 50 ml Vial.
Methotrexate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, handler-protective Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the antimetabolite.
Active Ingredient Strength Primary Clinical Function Methotrexate USP/Ph.Eur. 2.5 mg Global Autoimmune Standard: The absolute foundational unit for Rheumatoid Arthritis and Psoriasis, allowing for highly precise, incremental dose titration. Methotrexate USP/Ph.Eur. 5 mg / 7.5 mg / 10 mg Escalated / Oncology Standard: Higher-dose units for severe, refractory autoimmune disease, Choriocarcinoma, and maintenance therapy in Acute Lymphoblastic Leukemia (ALL). Excipients Lactose Monohydrate / Maize Starch / Pregelatinized Starch / Magnesium Stearate Diluent / Binder / Disintegrant / Lubricant (Engineered specifically using high-containment wet granulation to prevent airborne cytotoxic dust generation during manufacturing, ensuring precise, even API distribution) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, heavily monitored chronic dispensing regimens).
Methoxsalen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Dissolution Tablet or Liquid-Filled Softgel, packed exclusively in highly secure, light-blocking Alu-PVC or Amber Blister strips to ensure the absolute chemical stability of the highly photoactive molecule.
Active Ingredient Strength Primary Clinical Function Methoxsalen (8-Methoxypsoralen) USP/Ph.Eur. 10 mg Global Phototherapy Standard: Weight-based dosing unit designed for exact pharmacokinetic synchronization with scheduled clinical UVA light exposure. Excipients Microcrystalline Cellulose / Pregelatinized Starch / Colloidal Silicon Dioxide / Magnesium Stearate (If Tablet) OR Macrogol (PEG 400) / Gelatin (If Softgel) Fast-Dissolving Carrier / Disintegrant / Glidant (Engineered specifically to guarantee complete gastric breakdown and maximum systemic absorption within 60 to 90 minutes, ensuring the patient is perfectly “primed” for the light booth) *Pack Sizes: Bottles of 30 or 10×10 Blisters (Optimized specifically for strict, monitored bi-weekly dermatological dispensing regimens).
Methyl Cobalmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Rapid-Melt Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of both the delicate coenzyme and the hyper-hygroscopic ODT matrix.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Mecobalamin) Ph.Eur./USP 1500 mcg Global Neurology Standard: Mega-dose adult therapy for the aggressive regeneration of peripheral nerves and immediate correction of severe B12 anemia. Excipients Mannitol / Crospovidone / Microcrystalline Cellulose / Sucralose / Premium Cherry or Berry Flavoring / Magnesium Stearate Fast-Dissolving Carrier / Superdisintegrant / Diluent / Sweetener / Masking Agent (Engineered specifically to instantly melt in the saliva within 10 to 30 seconds, creating a highly palatable, sweet liquid that diffuses instantly into the sublingual capillaries) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology and diabetic dispensing regimens).
Methylcobalamin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Red Solution in amber glass ampoules.
Active Ingredient Strength Volume Methylcobalamin JP/USP 500 mcg 1 ml Ampoule Methylcobalamin JP/USP 1500 mcg (1.5 mg) 1 ml / 2 ml Ampoule (Standard Adult Dose) Methylcobalamin JP/USP 2500 mcg (2.5 mg) High-Dose (Intensive Therapy) Excipients Mannitol / Benzyl Alcohol Stabilizer / Preservative *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 100 Ampoules.
Methylcobalamin, Folic Acid & Pyridoxine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the three distinct vitamin coenzymes.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Active B12) Ph.Eur./USP 1500 mcg Myelin Regenerator: Direct peripheral nerve repair and essential co-factor for homocysteine remethylation. Folic Acid (Vitamin B9) Ph.Eur./USP 5 mg Endothelial Shield: Mega-dose methyl-donor driving DNA synthesis, red blood cell formation, and toxic homocysteine clearance. Pyridoxine Hydrochloride (Vitamin B6) Ph.Eur./USP 3 mg Neurotransmitter Catalyst: Vital co-enzyme for the transsulfuration of homocysteine and the synthesis of GABA/Serotonin. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / Heavy UV-Blocking Coating (Engineered specifically to form an impenetrable light barrier, completely preventing the photolabile degradation of the B12 component) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology dispensing regimens).
Methylcobalamine Folic Acid Pyridoxine Hydrochloride & DHA Capsules
FreeThis combination is a specialized nutritional supplement, often prescribed for nerve health (neuropathy), pregnancy, or cardiovascular support. It combines essential B-vitamins with a crucial fatty acid.Methylcobalamine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the delicate coenzyme.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Mecobalamin) Ph.Eur./USP 500 mcg Maintenance / Hematology Standard: Base therapeutic unit for the treatment of Megaloblastic/Pernicious anemia and general nutritional B12 deficiency. Methylcobalamin (Mecobalamin) Ph.Eur./USP 1500 mcg Global Neurology Standard: Mega-dose adult therapy for the aggressive regeneration of peripheral nerves in Diabetic Neuropathy, Sciatica, and Trigeminal Neuralgia. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / UV-Blocking Coating (Engineered specifically to form a heavy, opaque shield that completely locks out ultraviolet light, preventing the photolabile degradation of the active coenzyme) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology dispensing regimens).
Methylprednisolone Acetate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Milky White Suspension in glass vials.
Active Ingredient Strength Standard Use Methylprednisolone Acetate 40 mg / ml Standard IM / Small Joints Methylprednisolone Acetate 80 mg / ml High Dose IM / Large Joints (Knee) Excipients Polyethylene Glycol (PEG) / Myristyl-gamma-picolinium chloride Suspending Agent / Preservative *Pack Sizes: 1 ml Vial, 2 ml Vial, or 5 ml Multi-dose Vial.
Methylprednisolone Sodium Succinate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder requiring reconstitution with the provided solvent.
Active Ingredient Strength Standard Use Methylprednisolone Sod. Succ. 40 mg Local Injection / Minor Allergic Reaction Methylprednisolone Sod. Succ. 125 mg Acute Asthma / Status Asthmaticus Methylprednisolone Sod. Succ. 500 mg / 1000 mg (1 gm) Pulse Therapy (Lupus / Transplant Rejection) Diluent Bacteriostatic Water Provided with Act-O-Vial or Separate Ampoule *Pack Sizes: Single Vial with Diluent.
Metoclopramide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Isotonic Solution in glass ampoules.
Active Ingredient Strength Volume Metoclopramide HCl USP/BP 5 mg / ml 2 ml Ampoule (Total 10 mg) Metoclopramide HCl USP/BP 5 mg / ml 10 ml Multi-dose Vial Preservative Sodium Metabisulfite Antioxidant *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Metoprolol & Amlodipin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the combined molecules.
Active Ingredient Strength Primary Clinical Function Metoprolol (as Tartrate/Succinate ER) Ph.Eur./USP 25 mg / 50 mg Cardioselective Base: Reduces heart rate, cardiac workload, and neutralizes CCB-induced reflex tachycardia. Amlodipine (as Besylate) Ph.Eur./USP 5 mg Calcium Channel Blocker (CCB): Forces profound peripheral arterial vasodilation, dropping severe blood pressure and relieving coronary spasms. Excipients Microcrystalline Cellulose / Dibasic Calcium Phosphate / Crospovidone / Magnesium Stearate / Premium Opadry Film / Iron Oxide Colors Diluent / Stabilizing Buffer / Superdisintegrant / Lubricant (Engineered specifically using bilayer press technology to physically separate the slightly acidic Metoprolol salt from the basic Amlodipine, preventing destructive chemical cross-talk) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Metoprolol & Ramipril Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly degradable Ramipril molecule.
Active Ingredient Strength Primary Clinical Function Metoprolol (as Succinate/Tartrate) Ph.Eur./USP 25 mg / 50 mg Cardioselective Base: Reduces heart rate, cardiac output, and myocardial oxygen demand; protects against sudden cardiac death. Ramipril Ph.Eur./USP 2.5 mg / 5 mg ACE Inhibitor Driver: Forces profound systemic vasodilation, protects the kidneys (renoprotection), and halts pathological cardiac remodeling. Excipients Microcrystalline Cellulose / Sodium Stearyl Fumarate / Hypromellose / Sodium Bicarbonate / Iron Oxide Colors Low-Moisture Diluent / Lubricant / Film-Coating / Polymeric Stabilizer (Engineered specifically to physically isolate the acidic Ramipril from cross-reacting with the Metoprolol salt, preventing the formation of toxic diketopiperazine impurities) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Metronidazole Capsule 500mg
FreeMetronidazole 500 mg capsules are an antibiotic and antiprotozoal medication used to treat a variety of bacterial and parasitic infections. The capsule contains a specific amount of the active drug and various inactive ingredients that help with its delivery and stability.
Metronidazole Vaginal Tablets
FreeProduct Composition & Strength
We supply this product as compressed Vaginal Tablets (Pessaries) in blister packs.
Active Ingredient Strength (Standard) Form Role Metronidazole IP/BP/USP 500 mg Uncoated / Film Coated Tablet Antiprotozoal / Antibacterial Lactic Acid Q.S. (Optional Additive) pH Regulator Excipients Q.S. Disintegrants / Binders Base for Tablet Midazolam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Immediate-Release Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly soluble maleate salt.
Active Ingredient Strength Primary Clinical Function Midazolam (as Maleate) Ph.Eur./USP 7.5 mg Initiation / Geriatric Standard: Base therapeutic unit for pre-surgical anxiety reduction and sleep induction in elderly or debilitated patients. Midazolam (as Maleate) Ph.Eur./USP 15 mg Global Anesthesiology Standard: High-efficacy adult dose for profound pre-procedural conscious sedation and the treatment of severe, treatment-refractory insomnia. Excipients Microcrystalline Cellulose / Lactose Anhydrous / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Fast-Dissolving Carrier / Superdisintegrant / Lubricant (Engineered specifically to shatter upon contact with gastric fluid, ensuring peak plasma concentration is reached within 20 to 30 minutes) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, highly monitored hospital and short-term dispensing regimens).
Midodrine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Immediate-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly soluble hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Midodrine (as Hydrochloride) USP/Ph.Eur. 2.5 mg / 5 mg Initiation / Titration Standard: Base therapeutic units for careful dose-titration to elevate standing blood pressure without triggering dangerous supine hypertension. Midodrine (as Hydrochloride) USP/Ph.Eur. 10 mg Global Dysautonomia Standard: High-efficacy adult maintenance dose for severe neurogenic orthostatic hypotension. Excipients Microcrystalline Cellulose / Pregelatinized Starch / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Disintegrant / Glidant / Lubricant (Engineered specifically without heavy polymeric retardants to guarantee rapid, complete gastric dissolution, ensuring the prodrug reaches the liver instantly for conversion) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, daytime-only chronic dispensing regimens).
Mifepristone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active synthetic steroid.
Active Ingredient Strength Primary Clinical Function Mifepristone (RU-486) Ph.Eur./USP 200 mg Global Reproductive Standard: High-dose adult therapy for the initiation of medical termination of early intrauterine pregnancy (typically up to 70 days gestation). Excipients Microcrystalline Cellulose / Povidone K30 / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant (Engineered specifically to ensure rapid, complete disintegration in the acidic gastric environment, guaranteeing maximum systemic absorption of the critical 200mg payload) *Pack Sizes: 1-Tablet Blister Packs (Optimized specifically for strict, highly regulated single-dose clinical dispensing protocols).
Minocycline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix ER Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or opaque HDPE bottles to ensure the absolute chemical stability of the photosensitive hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Minocycline (as Hydrochloride) USP/Ph.Eur. 50 mg (ER) Dermatology Maintenance Standard: Long-term, low-dose therapy for controlling inflammatory acne and severe Rosacea with minimal side effects. Minocycline (as Hydrochloride) USP/Ph.Eur. 100 mg (ER) Acute Clearance Standard: High-dose therapy for severe cystic acne breakouts, CA-MRSA skin infections, and Rheumatoid Arthritis flares. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Magnesium Stearate / Premium Opaque Opadry Film Hydrophilic ER Polymer / Diluent / Lubricant / UV-Blocking Coating (Engineered specifically to pace the gastric release over several hours, preventing the rapid blood-brain-barrier saturation that triggers vertigo) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 12-to-16 week chronic dermatology dispensing regimens).
Mirabegron Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix ER Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute physical stability of the extended-release polymers.
Active Ingredient Strength Primary Clinical Function Mirabegron Ph.Eur./USP 25 mg (ER) Initiation / Renal Standard: Base therapeutic unit for assessing patient tolerance and for use in patients with severe renal or hepatic impairment. Mirabegron Ph.Eur./USP 50 mg (ER) Global Urology Standard: High-efficacy adult maintenance therapy for maximum suppression of urge urinary incontinence and detrusor overactivity. Excipients Polyethylene Oxide / Hypromellose (HPMC) / Butylated Hydroxytoluene (BHT) / Magnesium Stearate / Premium Opadry Film Swellable ER Polymer / Hydrophilic Matrix Base / Antioxidant / Lubricant (Engineered specifically to form an impenetrable, slow-eroding gel matrix in the GI tract, strictly metering the release of the active ingredient over 24 hours) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic urology dispensing regimens).
Mirtazapine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the tetracyclic compound.
Active Ingredient Strength Primary Clinical Function Mirtazapine Ph.Eur./USP 15 mg Initiation / Maximum Sedation Standard: Base unit. (Clinical Quirk: Due to histamine saturation, the 15mg dose is actually MORE sedating than the higher doses, making it the primary choice for severe insomnia.) Mirtazapine Ph.Eur./USP 30 mg / 45 mg Global Psychiatry Standard: High-efficacy adult maintenance therapy for severe Major Depressive Disorder (MDD). At these doses, increased norepinephrine release counteracts some of the histamine-induced sedation. Excipients Microcrystalline Cellulose / Crospovidone / Mannitol / Aspartame / Magnesium Stearate / Premium Flavoring Diluent / Superdisintegrant / Sweetening Agent / Lubricant (Engineered specifically for rapid gastric or sublingual dissolution, heavily utilizing artificial sweeteners and flavors to completely mask the intensely bitter API for geriatric compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic psychiatric dispensing regimens).
Mitomycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (Purple/Blue Cake) in amber glass vials.
Active Ingredient Strength Primary Use Mitomycin USP/BP 2 mg Ophthalmic Surgery / Pterygium Mitomycin USP/BP 10 mg Systemic Chemotherapy / Bladder Instillation Mitomycin USP/BP 20 mg / 40 mg High-Dose Bladder Protocols Excipients Mannitol Bulking Agent *Pack Sizes: Single Vial. (Must be handled with cytotoxic precautions).
Morphine Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extended-Release Matrix Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the controlled-release polymers.
Active Ingredient Strength Primary Clinical Function Morphine Sulphate USP/Ph.Eur. 15 mg (SR) Initiation / Titration Standard: Base therapeutic unit for opioid-naïve patients starting around-the-clock chronic pain management. Morphine Sulphate USP/Ph.Eur. 30 mg / 60 mg (SR) Global Oncology Standard: High-dose adult maintenance therapy for severe, opioid-tolerant terminal cancer and intractable neuropathic pain. Excipients Hypromellose (HPMC) / Cetostearyl Alcohol / Lactose Monohydrate / Magnesium Stearate / Premium Color-Coded Film Hydrophilic Polymer / Lipophilic Retardant / Diluent / Lubricant (Engineered specifically to form an impenetrable, slow-eroding gel matrix in the GI tract, strictly metering the release of the narcotic over 12 hours) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic oncology dispensing regimens; frequently color-coded by strength to prevent fatal dispensing errors).
Moxifloxacin & Cefixime Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive antibiotic compounds.
Active Ingredient Strength Primary Clinical Function Moxifloxacin (as Hydrochloride) Ph.Eur./USP 400 mg 4th-Gen Fluoroquinolone: Deep tissue and lung penetration to eradicate DNA replication in resistant respiratory and intra-abdominal pathogens. Cefixime (as Trihydrate) Ph.Eur./USP 400 mg 3rd-Gen Cephalosporin: Massive Gram-negative cell wall destruction, specifically targeting enteric pathogens like Salmonella typhi. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to protect the hygroscopic Cefixime Trihydrate and mask the intensely bitter taste of Moxifloxacin) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 7-to-14 day acute critical-care anti-infective dispensing regimens).
Moxifloxacin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Moxifloxacin (as Hydrochloride) Ph.Eur./USP 400 mg Global Pulmonology Standard: High-dose adult therapy for the aggressive eradication of resistant respiratory, skin, and intra-abdominal pathogens. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Lactose Monohydrate / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to protect the highly hygroscopic API and completely mask its intensely bitter taste) *Pack Sizes: 1×5 or 10×10 Alu-Alu Blisters (Optimized specifically for strict 5-to-14 day acute critical-care dispensing regimens).
Moxonidine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Micro-Dosed Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient.
Active Ingredient Strength Primary Clinical Function Moxonidine Ph.Eur./BP 0.2 mg Initiation / Mild Standard: Base therapeutic unit for starting therapy, specifically titrated to assess patient tolerance and prevent initial hypotension. Moxonidine Ph.Eur./BP 0.3 mg / 0.4 mg Global Cardiology Standard: High-efficacy adult maintenance dose for the aggressive management of resistant and metabolic hypertension. Excipients Lactose Monohydrate / Povidone K30 / Crospovidone / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Lubricant (Engineered specifically using strict geometric dilution protocols to ensure the microscopic API dose is flawlessly and evenly distributed throughout the entire tablet batch) *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict chronic cardiology dispensing regimens).
Multivitamin & Multimineral Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Sugar Coated Tablets (typically Red, Maroon, or Brown). The coating is an absolute necessity to prevent the oxidative degradation of vitamins by the mineral salts.
Category Ingredient (BP Grade) Strength (Standard) Fat-Soluble Vitamins Vitamin A (Retinol Acetate/Palmitate) BP 2500 IU / 5000 IU Vitamin D3 (Cholecalciferol) BP 200 IU / 400 IU Vitamin E (Tocopheryl Acetate) BP 10 mg / 15 IU Water-Soluble Vitamins Vitamin B1 (Thiamine Mononitrate) BP 2 mg / 10 mg Vitamin B2 (Riboflavin) BP 2 mg / 10 mg Vitamin B3 (Nicotinamide) BP 25 mg / 50 mg Vitamin B6 (Pyridoxine HCl) BP 1 mg / 3 mg Vitamin B12 (Cyanocobalamin) BP 1 mcg / 15 mcg Folic Acid BP 1 mg Vitamin C (Ascorbic Acid) BP 50 mg / 100 mg Minerals & Trace Elements Ferrous Fumarate / Sulphate BP 30 mg / 50 mg (Elemental Iron) Zinc Sulphate BP 15 mg (Elemental Zinc) Copper Sulphate BP 0.5 mg / 2 mg Selenium (as Sodium Selenite) BP 60 mcg / 70 mcg Iodine (as Potassium Iodide) BP 100 mcg / 150 mcg Multivitamin & Multimineral Tablets (Complete A-Z Formula)
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Red, Maroon, or Brown). The coating is an absolute necessity to prevent the oxidative degradation of vitamins by the mineral salts.
Category Ingredient Strength (Standard) Fat-Soluble Vitamins Vitamin A (Acetate/Palmitate) 2500 IU / 5000 IU Vitamin D3 (Cholecalciferol) 200 IU / 400 IU Vitamin E (Acetate) 10 mg / 15 mg Water-Soluble Vitamins Vitamin B1 (Thiamine Mononitrate) 2 mg / 10 mg Vitamin B2 (Riboflavin) 2 mg / 10 mg Vitamin B6 (Pyridoxine HCl) 1 mg / 3 mg Vitamin B12 (Cyanocobalamin) 1 mcg / 15 mcg Vitamin C (Ascorbic Acid) 50 mg / 100 mg Nicotinamide (Vit B3) 25 mg / 50 mg Folic Acid (Vit B9) 1000 mcg (1 mg) Minerals & Trace Elements Ferrous Sulphate (Iron) 30 mg / 50 mg (Elemental) Zinc Sulphate Monohydrate 15 mg / 22.5 mg (Elemental) Copper Sulphate 0.5 mg / 2 mg Selenium Dioxide 60 mcg / 70 mcg Potassium Iodide 100 mcg / 150 mcg Multivitamin 4G Softgels
Free4G multivitamin softgels are specialized health supplements that get their “4G” name from four key herbal extracts—Ginseng, Green Tea, Ginkgo Biloba, and Grape Seed—combined with Omega-3 fatty acids and a comprehensive range of vitamins and minerals. These softgels are designed to support cardiovascular health, cognitive function, and immunity.
Multivitamin Injection
FreeProduct Composition & Strength
We supply this product as a Dual-Ampoule Set or a Single-Vial Emulsion (depending on market regulation).
Vitamin Group Active Ingredients Standard Adult Dose (per 10 ml) Fat-Soluble Retinol (A) / Ergocalciferol (D) / Tocopherol (E) 3300 IU / 200 IU / 10 IU Water-Soluble (C) Ascorbic Acid (C) 100 mg – 200 mg Water-Soluble (B) Thiamine (B1) / Riboflavin (B2) / Pyridoxine (B6) 3 mg / 3.6 mg / 4 mg Others Niacinamide / Pantothenic Acid / Folic Acid / B12 / Biotin 40 mg / 15 mg / 400 mcg / 5 mcg / 60 mcg *Pack Sizes: Tray of 5 Dual-Ampoules or Box of 10 Vials.
Multivitamin Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (typically Red, Yellow, or Brown). The sugar coating is mandatory to mask the strong odor of B-vitamins and protect the labile Vitamin A and C from oxidation.
Active Ingredient Strength (Standard IP/NFI) Therapeutic Role Vitamin A (Acetate) IP 2500 IU Vision / Immunity Vitamin B1 (Thiamine Mononitrate) IP 2 mg Carbohydrate Metabolism Vitamin B2 (Riboflavin) IP 2 mg Mucosal Health Vitamin B6 (Pyridoxine HCl) IP 1 mg Protein Synthesis Niacinamide IP 25 mg Cellular Energy Calcium Pantothenate IP 5 mg Metabolic Support Vitamin C (Ascorbic Acid) IP 50 mg Antioxidant / Collagen Vitamin D3 (Cholecalciferol) IP 200 IU Bone Mineralization Folic Acid IP 1 mg DNA Synthesis / Anemia Excipients Q.S. Gelatin / Sucrose / Talc Binder / Coating Multivitamin Tablets (Vitamin A, D3 & B-Complex)
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (typically Red, Yellow, or Brown). The sugar coating is critical to mask the strong odor of B-vitamins and protect Vitamin A from oxidation.
Active Ingredient Strength (Standard Prophylactic) Therapeutic Role Vitamin A (Acetate/Palmitate) 2500 IU / 5000 IU Vision / Immunity Vitamin D3 (Cholecalciferol) 200 IU / 400 IU Bone Mineralization Thiamine Mononitrate (Vit B1) 2 mg / 10 mg Nerve Function Riboflavin (Vit B2) 2 mg / 10 mg Cellular Energy Pyridoxine HCl (Vit B6) 1 mg / 3 mg Protein Metabolism Niacinamide 20 mg / 50 mg Skin Health / Energy Calcium Pantothenate 5 mg / 50 mg Metabolic Support Folic Acid 1 mg / 1.5 mg DNA Synthesis Excipients Q.S. Gelatin / Sucrose / Talc Binder / Coating Multivitamin Vitamin & B Complex Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often Red, Maroon, or Yellow) to mask the taste and odor of minerals.
Category Key Ingredients (Standard A-Z Profile) Fat Soluble Vitamins Vitamin A (2500 IU), Vitamin D3 (200 IU), Vitamin E (10 mg) Water Soluble Vitamins Vitamin C (50 mg), B1 (2 mg), B2 (2 mg), B6 (1.5 mg), B12 (1 mcg), Niacinamide (25 mg), Folic Acid (300 mcg), Calcium Pantothenate (5 mg) Essential Minerals Zinc Sulfate (Eq. 10 mg Zinc), Ferrous Fumarate (Eq. 30 mg Iron), Magnesium Oxide (10 mg), Calcium Carbonate (75 mg) Trace Elements Copper, Manganese, Iodine, Selenium (Q.S.) Multivitamins & Multiminerals Capsules
FreeMultivitamin and multimineral capsules contain a broad spectrum of active nutrients designed to fill dietary gaps, along with inactive excipients that provide structure and stability to the capsule. While specific formulations vary by brand and target audience (such as men, women, or seniors), most contain a combination of 13 essential vitamins and several key minerals.
Mycophenolate Mofetil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant and handler-protective Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Mycophenolate Mofetil USP/Ph.Eur. 250 mg Dose-Titration / Pediatric Standard: Base therapeutic unit for precise plasma-level titration and pediatric transplant management. Mycophenolate Mofetil USP/Ph.Eur. 500 mg Global Transplant Standard: High-dose adult maintenance therapy for the aggressive prevention of solid organ rejection. Excipients Microcrystalline Cellulose / Povidone K-90 / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Heavy Film-Coating (Engineered specifically to create a dense, impenetrable barrier over the cytotoxic API core, ensuring absolute handling safety for nurses and pharmacists) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic post-transplant dispensing regimens).
N-Acetyl Cysteine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Effervescent Tablet or Odor-Masked Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge Alu-Alu or Strip packs to ensure the absolute chemical stability of the highly hygroscopic API.
Active Ingredient Strength Primary Clinical Function N-Acetyl Cysteine (NAC) USP/Ph.Eur. 600 mg Global Pulmonology Standard: High-dose adult therapy for the rapid liquefaction of thick respiratory mucus and systemic antioxidant replenishment. Excipients (Effervescent Matrix) Citric Acid Anhydrous / Sodium Bicarbonate / Sucralose / Premium Orange-Lemon Flavoring / Macrogol 6000 Acid-Base Effervescent Couple / Sweetener / Odor-Masking Flavor / Lubricant (Engineered specifically to trigger a violent, complete dissolution in water within 60 seconds, creating a clear, pleasant-tasting respiratory therapeutic drink) *Pack Sizes: 10-Tablet Tubes, 10×10 Strip Packs, or Alu-Alu Blisters (Optimized specifically to absolutely lock out ambient moisture).
N-Acetylcysteine & Taurine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Odor-Masked Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic and sulfurous active ingredients.
Active Ingredient Strength Primary Clinical Function N-Acetylcysteine (NAC) USP/Ph.Eur. 150 mg Glutathione Precursor: Rapid neutralization of reactive oxygen species (ROS) to protect renal tubules and hepatic lobules. Taurine USP/Ph.Eur. 500 mg Intracellular Osmoregulator: Stabilization of glomerular cell membranes to prevent apoptosis and halt proteinuria. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Vanilla-Flavored Opadry Film Diluent / Superdisintegrant / Glidant / Heavy Odor-Masking Coating (Engineered specifically to lock in the noxious sulfur smell of NAC, ensuring absolute patient compliance for long-term chronic use) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic nephrology dispensing regimens).
Naloxone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Pre-filled Syringes.
Active Ingredient Strength Format Naloxone Hydrochloride USP/BP 400 mcg (0.4 mg) 1 ml Ampoule (Standard Adult) Naloxone Hydrochloride USP/BP 20 mcg (0.02 mg) 1 ml Ampoule (Neonatal/Pediatric) Excipients Methylparaben / Propylparaben Preservative (in Multi-dose Vials) *Pack Sizes: Tray of 10 Ampoules or Box of 10 Vials.
Naltrexone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Taste-Masked Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Naltrexone Hydrochloride USP/Ph.Eur. 50 mg Global Addiction Standard: Single daily maintenance dose to ensure continuous, 24-hour blockade of opioid receptors and suppression of alcohol cravings. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Crospovidone / Magnesium Stearate / Colloidal Silicon Dioxide / Premium Opadry Film Diluent / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically to completely mask the violently bitter taste of the API, preventing the patient from spitting the pill out and ensuring total compliance) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for strictly monitored, 30-day outpatient rehabilitation dispensing regimens).
Naproxen Sodium Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the hygroscopic sodium salt.
Active Ingredient Strength Primary Clinical Function Naproxen Sodium USP/Ph.Eur. 275 mg
(Equivalent to 250 mg Naproxen base)Acute Mild / OTC Standard: Base therapeutic unit for rapid relief of tension headaches, mild trauma, and OTC fever reduction. Naproxen Sodium USP/Ph.Eur. 550 mg
(Equivalent to 500 mg Naproxen base)Acute Severe Rx Standard: High-dose “loading” therapy to instantly abort severe acute migraines, acute gout flares, and post-surgical pain. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Talc / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to protect the hygroscopic salt from humidity in the blister, but trigger a violent, immediate structural collapse the exact second it hits the stomach) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-turnover acute dispensing and retail pharmacy OTC placement).
Naproxen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient and the protective polymer matrix.
Active Ingredient Strength Primary Clinical Function Naproxen USP/Ph.Eur. 250 mg (EC) Initiation / Mild Standard: Base therapeutic unit for mild musculoskeletal trauma, acute gout, and primary dysmenorrhea. Naproxen USP/Ph.Eur. 500 mg (EC) Global Rheumatology Standard: High-dose adult maintenance therapy for severe Rheumatoid Arthritis, Osteoarthritis, and Ankylosing Spondylitis. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Triethyl Citrate / Magnesium Stearate pH-Dependent Enteric Barrier / Diluent / Superdisintegrant / Plasticizer (Engineered specifically to absolutely block dissolution in the highly acidic stomach, preventing mucosal burns, and rapidly dissolving only in the alkaline duodenum) *Pack Sizes: 10×10 Blisters or Bottles of 100/500 (Optimized specifically for strict chronic orthopedic dispensing regimens and massive government health tenders).
Nateglinide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Disintegrating Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly soluble API.
Active Ingredient Strength Primary Clinical Function Nateglinide Ph.Eur./USP 60 mg Initiation / Mild Standard: Base therapeutic unit for patients nearing their HbA1c goal who only require mild postprandial glycemic control. Nateglinide Ph.Eur./USP 120 mg Global Clinical Standard: Primary adult maintenance dose for severe meal-time spikes, taken immediately before the three main meals of the day. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Glidant (Engineered specifically to shatter and dissolve in the stomach in under 15 minutes, guaranteeing the insulin surge perfectly matches the digestion of the meal) *Pack Sizes: 3×10 or 10×10 Blisters (Optimized specifically for high-turnover diabetic dispensing, as patients consume 3 tablets per day).
Nebivolol & Telmisartan Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic and pH-sensitive active ingredients.
Active Ingredient Strength Primary Clinical Function Nebivolol (as HCl) Ph.Eur./USP 2.5 mg / 5 mg Nitric Oxide Donating Beta-Blocker: Reduces cardiac workload while promoting active peripheral vasodilation and preserving sexual function. Telmisartan Ph.Eur./USP 40 mg Metabolic ARB: Provides sustained 24-hour RAAS blockade and improves cellular insulin sensitivity (PPAR-γ modulation). Excipients Meglumine / Sodium Hydroxide / Microcrystalline Cellulose / Povidone K30 / Polysorbate 80 / Magnesium Stearate Alkalizing Agents (Meglumine) / Diluent / Binder / Surfactant (Engineered specifically to create a hyper-alkaline micro-environment for Telmisartan dissolution, physically isolated from the Nebivolol layer to prevent cross-degradation) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Nebivolol Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dual-Active Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the active ingredients.
Active Ingredient Strength Primary Clinical Function Nebivolol (as HCl) Ph.Eur./USP 5 mg Cardioselective & Vasodilatory Base: Reduces cardiac workload and provides active Nitric Oxide-driven peripheral vasodilation. Hydrochlorothiazide (HCTZ) Ph.Eur./USP 12.5 mg / 25 mg Thiazide Diuretic Driver: Forces the excretion of excess sodium and water, massively amplifying the blood-pressure-lowering effect of the beta-blocker. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Polysorbate 80 / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Wetting Surfactant / Moisture-Barrier Coating (Engineered specifically to protect the highly delicate racemic Nebivolol balance while ensuring rapid, synchronized gastric dissolution of the diuretic) *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Nebivolol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Dose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Nebivolol (as HCl) Ph.Eur./USP 2.5 mg / 5 mg Global Hypertension Standard: Base therapeutic unit for the continuous, highly tolerated management of essential hypertension. Nebivolol (as HCl) Ph.Eur./USP 10 mg / 20 mg Advanced Cardiac Standard: High-dose maintenance therapy for refractory hypertension and specialized heart failure protocols. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Hypromellose / Polysorbate 80 / Magnesium Stearate Diluent / Superdisintegrant / Wetting Agent / Lubricant (Engineered specifically to ensure rapid, predictable gastric dissolution while protecting the delicate racemic balance of the API) *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict, high-compliance chronic cardiology dispensing regimens).
Neomercazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly reactive thionamide molecule.
Active Ingredient Strength Primary Clinical Function Carbimazole Ph.Eur./BP 5 mg Maintenance / Titration Standard: Base therapeutic unit for the gradual tapering of therapy and long-term maintenance of euthyroidism. Carbimazole Ph.Eur./BP 10 mg / 20 mg Acute Initiation Standard: High-dose induction therapy to aggressively shut down severe, life-threatening thyrotoxicosis. Excipients Lactose Monohydrate / Maize Starch / Magnesium Stearate / Povidone K30 / Iron Oxide Yellow (for distinct clinical identification) Diluent / Binder / Lubricant (Engineered specifically for rapid, complete gastric dissolution to achieve peak methimazole blood levels within 1 to 2 hours) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict chronic endocrinology dispensing, as patients initiate on high doses and taper down over many months).
Neostigmine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Isotonic Solution in glass ampoules or vials.
Active Ingredient Strength Format Neostigmine Methylsulfate USP/BP 0.5 mg / ml 1 ml / 10 ml Vial (Standard) Neostigmine Methylsulfate USP/BP 2.5 mg / ml Concentrate (Rarely used) Excipients Phenol / Methylparaben Preservative (in Multi-dose Vials) *Pack Sizes: Tray of 10 Ampoules or Box of 1/10 Vials.
Neostigmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly hygroscopic bromide salt.
Active Ingredient Strength Primary Clinical Function Neostigmine Bromide Ph.Eur./USP 15 mg Global Clinical Standard: Base therapeutic oral unit for the continuous, meticulously spaced symptomatic management of Myasthenia Gravis. Excipients Lactose Monohydrate / Maize Starch / Povidone K30 / Talc / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered specifically for rapid, predictable gastric dissolution to ensure precise symptom control within 30 to 45 minutes of ingestion) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, high-volume chronic neurology dispensing, as patients may require up to 10-15 tablets per day in divided doses).
Niacinamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Purity Tablet, packed exclusively in highly secure, premium Alu-PVC blister strips or high-density HDPE aesthetic bottles to ensure the absolute chemical stability of the vitamin matrix.
Active Ingredient Strength Primary Clinical Function Niacinamide (Vitamin B3) USP/Ph.Eur. 500 mg Global Premium Dermatology Standard: High-dose adult therapy for systemic acne control, anti-aging ceramide synthesis, and hyperpigmentation reduction. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Stearic Acid / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Lubricant (Engineered specifically for rapid gastric dissolution to ensure peak systemic saturation and rapid delivery to the dermal layers) *Pack Sizes: 10×10 Blisters or Bottles of 60/100 (Optimized specifically for premium OTC retail and daily dermatological regimens).
Nicorandil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Shielded Tablet, packed exclusively in highly secure, heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the highly volatile active ingredient.
Active Ingredient Strength Primary Clinical Function Nicorandil Ph.Eur./BP 5 mg Initiation / Titration Standard: Base therapeutic unit for the mandatory slow-titration protocol required to build patient tolerance and prevent severe “nitrate headaches.” Nicorandil Ph.Eur./BP 10 mg / 20 mg Global Cardiology Standard: High-dose adult maintenance therapy for severe, refractory stable angina pectoris. Excipients Maize Starch / Croscarmellose Sodium / Stearic Acid / Mannitol Low-Moisture Diluent / Superdisintegrant / Lubricant (Engineered specifically without hygroscopic binders to guarantee the tablet remains perfectly dry and structurally intact throughout its shelf life) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic cardiology dispensing regimens).
Nicotinamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or high-density HDPE bottles to ensure the absolute chemical stability of the highly soluble vitamin amide.
Active Ingredient Strength Primary Clinical Function Nicotinamide (Niacinamide) USP/Ph.Eur. 250 mg Dermatology / Acne Standard: Base therapeutic unit for the systemic reduction of inflammatory skin lesions and mild nutritional supplementation. Nicotinamide (Niacinamide) USP/Ph.Eur. 500 mg Oncology Prophylaxis / Pellagra Standard: High-dose adult therapy for non-melanoma skin cancer prevention and acute pellagra eradication. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Stearic Acid / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Lubricant (Engineered specifically for rapid, complete gastric dissolution to ensure peak systemic NAD+ saturation within 1 to 2 hours) *Pack Sizes: 10×10 Blisters or Bottles of 60/100 (Optimized specifically for chronic, twice-daily dermatological dispensing regimens).
Nicotinic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the extended-release polymer.
Active Ingredient Strength Primary Clinical Function Nicotinic Acid (Niacin) USP/Ph.Eur. 500 mg (ER) Initiation / Titration Standard: Base therapeutic unit for the mandatory, slow 4-week dose titration protocol required to build patient tolerance. Nicotinic Acid (Niacin) USP/Ph.Eur. 1000 mg (ER) Global Cardiology Standard: High-dose adult maintenance therapy for severe mixed dyslipidemia and extreme hypertriglyceridemia. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Stearic Acid / Colloidal Silicon Dioxide / Premium Opadry Film Hydrophilic Polymer Matrix / Diluent / Lubricant / Glidant (Engineered specifically to form a viscous, highly controlled gel barrier upon swallowing, metering the API release precisely into the gastrointestinal tract over 8-12 hours) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict chronic cardiology dispensing regimens).
Nimesulide ,Paracetamol & Chlorzoxazone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of all three active ingredients.
Active Ingredient Strength Primary Clinical Function Nimesulide BP/Ph.Eur. 100 mg Preferential COX-2 NSAID: Rapid abortion of localized musculoskeletal inflammation and tissue swelling. Paracetamol (Acetaminophen) BP/Ph.Eur. 325 mg Central Analgesic: Synergistic pain threshold elevation and antipyretic control. Chlorzoxazone USP/Ph.Eur. 250 mg Central Muscle Relaxant: Direct inhibition of spinal reflex arcs to break severe, locked muscle spasms. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to trigger a violent, immediate structural collapse in the stomach, ensuring all three APIs are absorbed simultaneously for synchronized relief) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute dispensing to ensure patients do not exceed the mandated 15-day Nimesulide therapy limit).
Nimesulide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient.
Active Ingredient Strength Primary Clinical Function Nimesulide BP/Ph.Eur. 100 mg Global Acute Standard: High-efficacy adult therapeutic unit for the rapid, short-term abortion of acute inflammatory pain. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Docusate Sodium / Povidone K30 / Magnesium Stearate Diluent / Superdisintegrant / Wetting Surfactant / Binder (Engineered specifically to trigger a violent, immediate structural collapse in the stomach, maximizing the drug’s surface area for ultra-fast gastrointestinal absorption) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute dispensing to ensure patients do not exceed the mandated 15-day therapy limit).
Nimesulide, Paracetamol & Serratiopeptidase Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Multi-Particulate Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly delicate enzyme component.
Active Ingredient Strength Primary Clinical Function Nimesulide BP/Ph.Eur. 100 mg Preferential COX-2 NSAID: Rapid abortion of localized musculoskeletal inflammation and tissue pain. Paracetamol (Acetaminophen) BP/Ph.Eur. 325 mg Central Analgesic: Synergistic pain threshold elevation and antipyretic control. Serratiopeptidase (as Enteric-Coated Granules) 15 mg
(Equivalent to 30,000 Serratiopeptidase Units)Proteolytic Enzyme: Direct breakdown of fibrin and inflammatory exudate to physically drain severe localized edema. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate Enteric Polymer Shield / Diluent / Superdisintegrant / Binder (Engineered specifically to protect the enzyme from gastric acid while allowing the analgesics to dissolve instantly in the stomach) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute dispensing to ensure patients do not exceed the mandated 15-day Nimesulide therapy limit).
Nitrazepam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient and prevent unauthorized access.
Active Ingredient Strength Primary Clinical Function Nitrazepam BP/Ph.Eur. 5 mg Initiation / Elderly Standard: Base therapeutic unit for the short-term management of severe insomnia, specifically titrated for elderly patients to prevent next-day falls. Nitrazepam BP/Ph.Eur. 10 mg Severe Psychiatric Standard: Maximum adult dose to force sleep in highly agitated, refractory, or acutely manic patients. Excipients Lactose Monohydrate / Maize Starch / Microcrystalline Cellulose / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Binder / Disintegrant / Lubricant (Engineered specifically for rapid gastric dissolution, inducing sleep within 30 to 60 minutes of ingestion) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 2-to-4 week acute psychiatric dispensing regimens to prevent dependency).
Nitrofurantoin Tablets
FreeA Nitrofurantoin tablet is an antibiotic specifically used to treat and prevent urinary tract infections (UTIs), such as cystitis. It works by damaging the DNA of bacteria in the urinary tract.
Nitrofurantoin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Dual-Release Capsule or Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the nitrofuran compounds.
Active Ingredient Strength Primary Clinical Function Nitrofurantoin (Macrocrystals) USP/Ph.Eur. 50 mg Prophylactic / Pediatric Standard: Base therapeutic unit for long-term prevention of recurrent UTIs and pediatric dosing. Nitrofurantoin (Macrocrystals 25mg + Monohydrate 75mg) USP 100 mg Global Acute UTI Standard: Premium dual-release adult maintenance dose for the rapid eradication of acute uncomplicated cystitis. Excipients Carbomer 934P / Povidone K30 / Sugar Spheres / Talc / Magnesium Stearate / Titanium Dioxide Hydrophilic Polymer Matrix / Binder / Core Substrate / Glidant (Engineered specifically to form a viscous gel upon swallowing, pacing the gastric release perfectly to prevent nausea while ensuring maximum urinary concentration) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict 5-to-7 day acute urology dispensing regimens).
Nitroglycerin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Concentrate for Infusion in glass ampoules or vials. (Must be diluted).
Active Ingredient Strength Total Content Nitroglycerin USP/BP 5 mg/ml 25 mg (in 5 ml Ampoule) Nitroglycerin USP/BP 5 mg/ml 50 mg (in 10 ml Vial) Excipients Propylene Glycol / Ethanol Solubilizers (Volatile) *Pack Sizes: Tray of 5 Ampoules or 10 Vials.
Norethisterone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent steroid hormone.
Active Ingredient Strength Primary Clinical Function Norethisterone Ph.Eur./USP 5 mg Global Gynecology Standard: High-dose therapeutic unit for acute hemorrhage cessation, endometriosis suppression, and menstrual cycle manipulation. Excipients Lactose Monohydrate / Maize Starch / Magnesium Stearate / Povidone K30 Diluent / Binder / Lubricant (Engineered specifically for rapid gastric dissolution to halt acute uterine bleeding within 24-48 hours of the first dose) Pack Sizes: 10×10 Blisters or 3×10 Calendar Packs (Optimized specifically for strict cyclical gynecology dispensing regimens).
Norfloxacin & Tinidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips to ensure the absolute chemical stability of the highly photolabile active ingredients.
Active Ingredient Strength Primary Clinical Function Norfloxacin USP/Ph.Eur. 400 mg Aerobic Gut/UTI Standard: Broad-spectrum eradication of Gram-negative/positive bacteria driving acute gastroenteritis and genitourinary infections. Tinidazole USP/Ph.Eur. 600 mg Anaerobic/Protozoal Standard: Highly tolerable eradication of tissue-invasive amoebas, giardia, and pelvic anaerobes. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Hypromellose / Titanium Dioxide Diluent / Superdisintegrant / Binder / Premium Opaque Film-Coating (Engineered specifically to form an impenetrable barrier that completely masks the notoriously bitter, metallic taste of both APIs, guaranteeing patient compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 5-to-10 day acute anti-infective dispensing regimens).
Ofloxacin & Ornidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips to ensure the absolute chemical stability of the highly photolabile active ingredients.
Active Ingredient Strength Primary Clinical Function Ofloxacin USP/Ph.Eur. 200 mg Aerobic Standard: Broad-spectrum eradication of Gram-negative/positive bacteria driving acute gastroenteritis and genitourinary infections. Ornidazole INN/Ph.Eur. 500 mg Anaerobic/Protozoal Standard: Highly tolerable eradication of tissue-invasive amoebas, giardia, and surgical-site anaerobes. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K30 / Magnesium Stearate / Hypromellose / Titanium Dioxide Diluent / Superdisintegrant / Binder / Premium Opaque Film-Coating (Engineered specifically to form an impenetrable barrier that completely masks the notoriously bitter, metallic taste of both APIs, guaranteeing patient compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-5 day acute anti-infective dispensing regimens).
Ofloxacin & Satranidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the fluoroquinolone and nitroimidazole APIs.
Active Ingredient Strength Primary Clinical Function Ofloxacin USP/Ph.Eur. 200 mg Broad-spectrum fluoroquinolone for the eradication of aerobic bacterial pathogens. Satranidazole INN/Ph.Eur. 300 mg Premium nitroimidazole for the eradication of anaerobic bacteria and protozoa. Excipients Microcrystalline Cellulose / Crospovidone / Magnesium Stearate / Hypromellose Diluent / Superdisintegrant / Lubricant / Premium Film-Coating (Engineered to mask bitterness and ensure immediate gastric dissolution) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for standard 3-to-5 day acute gastrointestinal and pelvic infection regimens).
Olanzapine & Fluoxetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Capsule or Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly oxidative Olanzapine molecule.
Active Ingredient Strength Primary Clinical Function Olanzapine Ph.Eur./USP 3 mg / 6 mg / 12 mg Atypical Base: Modulates 5-HT2A/D2 receptors to stabilize severe mood swings and trigger prefrontal synergy. Fluoxetine (as HCl) Ph.Eur./USP 25 mg / 50 mg SSRI Driver: Forces a massive serotonin pool in the synaptic cleft to elevate refractory depressive lows. Excipients Pregelatinized Starch / Croscarmellose Sodium / Microcrystalline Cellulose / Magnesium Stearate / Opadry Film Moisture-Scavenging Diluent / Superdisintegrant / Binder / Premium Oxygen-Barrier Film-Coating (Engineered specifically to physically isolate the highly sensitive Olanzapine from cross-reacting with Fluoxetine) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic psychiatric dispensing regimens).
Olanzapine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (Yellow Cake) in glass vials.
Active Ingredient Strength Reconstitution Requirement Olanzapine BP/USP 10 mg Requires 2.1 ml of Sterile Water for Injection Excipients Lactose Monohydrate / Tartaric Acid Bulking Agent / Solubilizer *Pack Sizes: Single Vial. (Produces a clear, yellow solution upon reconstitution).
Olmesartan Medoxomil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly volatile ester prodrug.
Active Ingredient Strength Primary Clinical Function Olmesartan Medoxomil Ph.Eur./USP 20 mg Initiation / Global Standard: Standard adult starting and maintenance dose for the continuous control of essential hypertension. Olmesartan Medoxomil Ph.Eur./USP 40 mg Severe Refractory Standard: Maximum adult maintenance dose for patients requiring further reduction in blood pressure. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Hydroxypropyl Cellulose / Magnesium Stearate / Titanium Dioxide Low-Moisture Diluent / Binder / Lubricant / Premium Moisture-Barrier Film-Coating (Engineered specifically to lock out ambient humidity and prevent the premature hydrolysis of the medoxomil group prior to ingestion) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Olmesartan, Amlodipine & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of all three active ingredients across their entire shelf life.
Active Ingredient Strength Primary Clinical Function Olmesartan Medoxomil Ph.Eur./USP 20 mg / 40 mg ARB Base: Blocks the renin-angiotensin-aldosterone system (RAAS) and provides critical diabetic renoprotection. Amlodipine (as Besylate) Ph.Eur./USP 5 mg / 10 mg CCB Vasodilator: Forces profound, sustained peripheral arterial relaxation. Hydrochlorothiazide (HCTZ) Ph.Eur./USP 12.5 mg / 25 mg Diuretic Volume Controller: Flushes excess sodium/water and massively amplifies the efficacy of the ARB component. Excipients Silicified Microcrystalline Cellulose / Pregelatinized Starch / Croscarmellose Sodium / Magnesium Stearate / Opadry Protective Film Moisture-Scavenging Diluent / Binder / Superdisintegrant / Premium Film-Coating (Engineered specifically to physically isolate the highly sensitive Olmesartan ester from the alkaline Amlodipine salt to prevent cross-degradation) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Omeprazole & Domperidone Capsules
FreeOmeprazole and Domperidone capsules are a combination medication primarily containing two active salts to treat acid reflux and indigestion.
Omeprazole Capsules
FreeOmeprazole capsules typically contain enteric-coated pellets to prevent the stomach’s acid from breaking down the medication before it can be absorbed in the small intestine.
Omeprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Off-White Cake) in clear glass vials, typically accompanied by a specialized sterile solvent.
Active Ingredient Strength Reconstitution Requirement Omeprazole Sodium USP/BP 40 mg Requires provided 10 ml solvent or specific diluent Excipients Sodium Hydroxide / Disodium Edetate Alkalizing Agent / Stabilizer *Pack Sizes: Single Vial + 10 ml Solvent Ampoule, or Tray of 10 Vials.
Omeprazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Capsule or Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly acid-labile benzimidazole derivative.
Active Ingredient Strength Primary Clinical Function Omeprazole BP/USP/Ph.Eur. 10 mg OTC / Maintenance Standard: Approved unit for over-the-counter frequent heartburn relief and long-term remission maintenance of healed esophagitis. Omeprazole BP/USP/Ph.Eur. 20 mg Global Clinical Standard: Primary adult daily dose for active GERD, gastric ulcers, and standard H. pylori eradication protocols. Omeprazole BP/USP/Ph.Eur. 40 mg Severe Refractory Standard: High-dose therapy for severe erosive esophagitis, NSAID-induced bleeding ulcers, and Zollinger-Ellison Syndrome. Excipients Methacrylic Acid Copolymer / Hypromellose (HPMC) / Sugar Spheres / Macrogol / Titanium Dioxide pH-Dependent Enteric Coating / Sub-coating Barrier / Core Substrate / Plasticizer (Engineered specifically to resist gastric fluid at pH 1.2 but dissolve instantly at duodenal pH 6.8) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 100 (Optimized specifically for strict 14-to-28 day acute GI healing regimens).
Ondansetron Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Aqueous Solution in glass ampoules or vials.
Active Ingredient Concentration Total Content & Format Ondansetron (as HCl Dihydrate) 2 mg / ml 4 mg in 2 ml Glass Ampoule Ondansetron (as HCl Dihydrate) 2 mg / ml 8 mg in 4 ml Glass Ampoule Excipients Citric Acid / Sodium Citrate pH Buffer System (pH 3.3 to 4.0) *Pack Sizes: Tray of 5/10 Ampoules or Box of 50 Ampoules.
Ondansitron Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Flash-Dispersion ODT or Standard Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant peelable Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic ODT matrix.
Active Ingredient Strength Primary Clinical Function Ondansetron (as HCl Dihydrate) Ph.Eur./USP 4 mg (ODT / FCT) Pediatric & PONV Standard: Base therapeutic unit for post-operative nausea, severe pediatric gastroenteritis, and mild emetic triggers. Ondansetron (as HCl Dihydrate) Ph.Eur./USP 8 mg (ODT / FCT) Global Oncology Standard: High-dose adult maintenance therapy for highly emetogenic chemotherapy (CINV) and radiation therapy (RINV). Excipients (ODT Formulation) Mannitol / Crospovidone / Aspartame / Colloidal Silicon Dioxide / Premium Mint Flavoring Lyophilized Matrix / Superdisintegrant / Sweetener / Saliva-Stimulating Flavor (Engineered specifically to draw saliva into the tablet matrix, forcing a violent, sub-5-second structural collapse on the tongue without a bitter aftertaste) *Pack Sizes: 10×10 Peelable Alu-Alu Blisters (Optimized specifically for strict oncology and surgical dispensing regimens).
Orciprenaline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly soluble sulphate salt.
Active Ingredient Strength Primary Clinical Function Orciprenaline Sulphate BP/Ph.Eur. 10 mg Pediatric / Initiation Standard: Base therapeutic unit for pediatric asthma management and dose titration. Orciprenaline Sulphate BP/Ph.Eur. 20 mg Global Adult Standard: Maximum adult maintenance dose for severe, chronic obstructive pulmonary disease (COPD). Excipients Microcrystalline Cellulose / Lactose Monohydrate / Maize Starch / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Binder / Disintegrant / Lubricant (Engineered specifically for rapid gastric dissolution and fast systemic absorption, providing relief within 30 minutes of oral administration) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-turnover acute dispensing and massive government health tenders).
Orlicure
FreeOrlicure is a pharmaceutical medication primarily containing Orlistat (120 mg) as its active ingredient. It is used for the management of obesity and weight loss by blocking the absorption of dietary fats in the intestines
Orligal
FreeOrligal capsules are anti-obesity medications used for weight loss and management. They primarily contain Orlistat as the active ingredient, typically in a 120 mg strength.
Orlistat Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Micro-Pellet Capsule or Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the highly delicate API.
Active Ingredient Strength Primary Clinical Function Orlistat INN/Ph.Eur. 60 mg OTC / Retail Standard: Base therapeutic unit approved in many regions for over-the-counter (OTC) weight loss management in overweight adults. Orlistat INN/Ph.Eur. 120 mg Global Clinical Standard: Prescription-strength adult maintenance dose for clinical obesity (BMI > 30) and severe metabolic syndrome. Excipients (Capsule Pellets) Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Povidone / Talc Diluent / Superdisintegrant / Wetting Surfactant / Binder (Engineered specifically to maximize the dispersion of the API across the entire gastrointestinal lumen to maximize enzyme binding) *Pack Sizes: Bottles of 84/120 or 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic bariatric dispensing regimens, taken with every major meal).
Ornidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips to ensure the absolute chemical stability of the highly photolabile active ingredient.
Active Ingredient Strength Primary Clinical Function Ornidazole INN/Ph.Eur. 500 mg Global Clinical Standard: Base therapeutic unit for the rapid eradication of protozoal and anaerobic pathogens. Excipients Microcrystalline Cellulose / Maize Starch / Sodium Starch Glycolate / Hypromellose / Titanium Dioxide Diluent / Binder / Superdisintegrant / Premium Film-Coating (Engineered specifically to create an impenetrable barrier that completely masks the notoriously bitter, foul taste of the nitroimidazole API, ensuring flawless patient compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-10 day acute anti-infective dispensing regimens).
Oseltamivir Tablet
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Hard Gelatin Capsule, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the hygroscopic phosphate salt.
Active Ingredient Strength Primary Clinical Function Oseltamivir Phosphate USP/Ph.Eur. 75 mg (Equivalent to Oseltamivir free base) Global Standard: Target adult dose for rapid treatment and prophylaxis of Influenza A/B. Excipients Pregelatinized Starch / Croscarmellose Sodium / Povidone / Sodium Stearyl Fumarate Diluent / Superdisintegrant (Engineered for immediate gastric capsule rupture and rapid systemic absorption) *Pack Sizes: 1×10 Blisters (Optimized perfectly for the standard 5-day acute treatment regimen of two capsules daily).
Oxacillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Crystalline Powder buffered for stability in glass vials.
Active Ingredient Strength Sodium Content Oxacillin Sodium USP/BP 500 mg Approx. 1.4 mEq (32 mg) Oxacillin Sodium USP/BP 1000 mg (1 g) Approx. 2.8 mEq (64 mg) Oxacillin Sodium USP/BP 2000 mg (2 g) High-Dose Protocols Buffer Dibasic Sodium Phosphate Maintains pH upon reconstitution *Pack Sizes: Single Vial or Tray of 10/50 Vials. (Requires reconstitution with Sterile Water for Injection).
Oxaliplatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Aqueous Concentrate in glass vials. (Also available as Lyophilized Powder depending on market preference).
Active Ingredient Strength Volume Oxaliplatin USP/BP 5 mg / ml 10 ml Vial (Total 50 mg) Oxaliplatin USP/BP 5 mg / ml 20 ml Vial (Total 100 mg) Excipients Water for Injection Preservative-Free Solution *Pack Sizes: Single Vial. (Must be handled with strict cytotoxic precautions).
Oxybutynin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Polymeric Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE desiccant bottles to ensure the absolute chemical stability of the controlled-release hydrogel network.
Active Ingredient Strength Primary Clinical Function Oxybutynin Chloride USP/Ph.Eur. 5 mg (ER) Initiation Standard: Base once-daily titration unit for the gradual introduction of antimuscarinic therapy. Oxybutynin Chloride USP/Ph.Eur. 10 mg / 15 mg (ER) Global Clinical Standard: Advanced maintenance doses for severe, refractory Overactive Bladder and neurogenic detrusor overactivity. Excipients Hypromellose (HPMC) / Lactose Anhydrous / Macrogol (PEG) / Magnesium Stearate / Titanium Dioxide Hydrophilic Polymer Matrix / Diluent / Plasticizer / Premium Film-Coating (Engineered specifically to form a highly viscous external gel barrier upon swallowing, controlling the exact 24-hour drug diffusion rate) *Pack Sizes: Bottles of 30 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-compliance 30-day chronic urology dispensing regimens).
Pancreatin & L-Ornithine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the biological proteins and the highly hygroscopic amino acid.
Active Ingredient Strength Primary Clinical Function Pancreatin (Porcine Origin) Ph.Eur./USP 170 mg
(Standardized Lipase/Protease/Amylase)Gastrointestinal Standard: Intraluminal enzymatic digestion of complex macronutrients to reverse malabsorption. L-Ornithine (as L-Ornithine L-Aspartate / LOLA) 150 mg Hepatology Standard: Hepatic urea cycle activation for aggressive ammonia detoxification and liver regeneration. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Crospovidone / Magnesium Stearate Enteric Barrier Coating (for Pancreatin) / Diluent / Superdisintegrant (Engineered specifically to separate the amino acid from the enzymes and ensure targeted duodenal release of the biologicals) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-compliance chronic hepato-gastro dispensing regimens).
Pancreatin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Tablet or Hard Capsule (containing Enteric Minimicrospheres), packed exclusively in highly secure, moisture-resistant Alu-Alu blisters or desiccant-lined HDPE bottles to ensure the absolute stability of the biological proteins.
Active Ingredient Strength (Standardized USP Units) Primary Clinical Function Pancreatin (Porcine Origin) Ph.Eur./USP 10,000 Lipase Units
(approx. 33,200 Protease / 33,200 Amylase)Pediatric / Initiation Standard: Base therapeutic unit for pediatric Cystic Fibrosis patients and meal-snack titration. Pancreatin (Porcine Origin) Ph.Eur./USP 25,000 Lipase Units
(approx. 85,000 Protease / 74,700 Amylase)Global Clinical Standard: High-dose adult maintenance therapy for severe Exocrine Pancreatic Insufficiency and Pancreatectomy. Excipients Methacrylic Acid Copolymer / Macrogol / Simethicone / Microcrystalline Cellulose / Triethyl Citrate Enteric Barrier Coating / Plasticizer / Anti-Foaming Agent / Diluent (Engineered specifically to protect the biological extract from gastric acid and ensure rapid, synchronized dissolution in the duodenum) *Pack Sizes: Bottles of 100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-volume daily dispensing where patients may consume 3 to 10 units daily with every meal and snack).
Pantoprazole & Domperidone Capsules
FreePantoprazole and domperidone capsules are combination medications used to treat gastrointestinal conditions involving both excess acid and motility issues, such as GERD and peptic ulcers. They are most commonly available in a fixed-dose strength of 40 mg pantoprazole and 30 mg domperidone.
Pantoprazole & Domperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Dual-Release Capsule or Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly acid-labile Pantoprazole and the SR polymer network.
Active Ingredient Strength Primary Clinical Function Pantoprazole Sodium Sesquihydrate USP/Ph.Eur. 40 mg (Enteric-Coated) Global Clinical Standard: Profound, 24-hour suppression of gastric acid production. Domperidone Maleate BP/Ph.Eur. 30 mg (Sustained-Release) Continuous 24-hour peripheral prokinetic action to accelerate gastric emptying and prevent nausea. Excipients Methacrylic Acid Copolymer / Hypromellose (HPMC) / Mannitol / Magnesium Stearate Enteric Barrier Coating / Hydrophilic SR Polymer Matrix / Diluent (Engineered specifically to perfectly isolate the two APIs and control their entirely separate intestinal dissolution rates) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-compliance 14-to-28 day chronic gastroenterology dispensing regimens).
Pantoprazole And Levosulpiride Capsules
FreePantoprazole and levosulpiride capsules are a combination therapy used for gastrointestinal conditions where excess acid is accompanied by motility issues. They are most commonly available in a fixed-dose strength of 40 mg (enteric-coated) and 75 mg (sustained-release).Pantoprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Off-White Cake) in clear glass vials.
Active Ingredient Strength Reconstitution Requirement Pantoprazole Sodium USP/BP 40 mg Requires 10 ml of 0.9% Sodium Chloride Excipients Sodium Hydroxide / Edetate Disodium Alkalizing Agent / Stabilizer *Pack Sizes: Single Vial or Tray of 10 Vials. (Often packed with a 10 ml ampoule of 0.9% NaCl diluent).
Paracetamol & Caffeine Anhydrous Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets or Uncoated Tablets. The anhydrous caffeine allows for a harder, more durable tablet suitable for bulk transport.
Active Ingredient Strength (Standard) Strength (Extra Power) Technical Grade Paracetamol IP/BP/USP 500 mg 650 mg Micronized Caffeine Anhydrous IP/BP/USP 30 mg 50 mg / 65 mg Moisture Content < 0.5% Excipients Q.S. Starch / PVP K-30 Binder Paracetamol & caffeine tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Uncoated Tablets in blister packs. Multiple strength combinations are available.
Product Variant Paracetamol Content Caffeine (Anhydrous) Common Name Standard Extra 500 mg 30 mg Panadol Extra Generic High Caffeine 500 mg 65 mg Migraine Relief Forte Strength 650 mg 50 mg Extra Strength Paracetamol & Diclofenac Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White, Orange, or Red). The coating is non-enteric to ensure immediate disintegration.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/USP 325 mg / 500 mg Central Analgesic Diclofenac Potassium IP/USP 50 mg Rapid Anti-Inflammatory Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Binder / Super-Disintegrant Paracetamol & Diclofenac Sodium Tablets
FreeProduct Composition & Strength
We supply this product as Enteric Coated or Film Coated Tablets in blister packs.
Active Ingredient Strength (Standard) Role Diclofenac Sodium IP/BP/USP 50 mg Anti-inflammatory / Analgesic Paracetamol IP/BP/USP 500 mg Analgesic / Antipyretic Excipients Q.S. Binder / Disintegrant Paracetamol & Orphenadrine Citrate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets in blister packs. We offer both Standard and Forte strengths.
Product Variant Paracetamol Content Orphenadrine Citrate Common Name Standard Strength 450 mg 35 mg Norgesic Generic Forte Strength 650 mg 50 mg Norgesic Forte Generic Excipients Q.S. — Binder / Filler paracetamol caffeine phenylephrine cpm Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (often colored/shaped for brand differentiation). This is a “fixed-dose combination” optimized for adult efficacy.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 500 mg Fever & Pain Reducer Caffeine (Anhydrous) 30 mg Analgesic Booster / Alertness Phenylephrine HCl 5 mg / 10 mg Nasal Decongestant Chlorpheniramine Maleate 2 mg / 4 mg Antiallergic Paracetamol Diclo Sodium Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Enteric Coated Tablets (typically White, Orange, or Yellow). The coating protects the stomach from the direct irritation of Diclofenac.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/USP 500 mg / 325 mg Central Analgesic / Antipyretic Diclofenac Sodium IP/USP 50 mg Peripheral Anti-Inflammatory Excipients Q.S. Maize Starch / Magnesium Stearate / Talc Binder / Lubricant Paracetamol Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Iso-osmotic Solution ready for direct intravenous infusion.
Active Ingredient Concentration Total Content & Format Paracetamol BP/USP 10 mg / ml 1000 mg (1 g) in 100 ml Glass Bottle / FFS Plastic Bottle Paracetamol BP/USP 150 mg / ml 300 mg in 2 ml Glass Ampoule (IM/IV use) Excipients Mannitol / Cysteine Hydrochloride Isotonic Agent / Oxygen Scavenger (Antioxidant) *Pack Sizes: 100 ml Single Bottle or Box of 10 Ampoules.
Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Standard) or Film Coated/Caplets (Easy Swallow). We offer varying release profiles.
Active Ingredient Strength (Standard) Role Paracetamol IP/BP/USP 500 mg Global Standard Adult Dose Paracetamol IP/BP/USP 650 mg High Potency / Sustained Pain Paracetamol IP/BP/USP 1000 mg (ER) Extended Release (Osteoarthritis) Excipients Q.S. Starch (Binder) / Lubricant Paracetamol, Caffeine & Phenylephrine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Film Coated Tablets. The absence of an antihistamine makes this the ideal “Work-Safe” cold remedy.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 500 mg / 650 mg Fever & Pain Reducer Caffeine Anhydrous IP/BP/USP 30 mg Alertness / Analgesic Booster Phenylephrine HCl IP/BP/USP 5 mg / 10 mg Nasal Decongestant Excipients Q.S. Povidone / Starch / MCC Paracetamol, Caffeine, Phenylephrine HCl & CPM Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Film Coated Tablets (often colored Red, Blue, or Bi-layered). The formulation is balanced for adult physiology.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 500 mg Fever & Pain Reducer Caffeine Anhydrous IP/BP/USP 30 mg Analgesic Potentiator / Alertness Phenylephrine HCl IP/BP/USP 5 mg / 10 mg Nasal Decongestant Chlorpheniramine Maleate IP/BP/USP 2 mg / 4 mg Antiallergic / Antihistamine Excipients Q.S. Starch / MCC / Colorants Paracetamol, Diclofenac Potassium & Caffeine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often capsule-shaped). The coating masks the bitter taste of Caffeine and the astringency of Diclofenac.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 325 mg / 500 mg Central Analgesic / Antipyretic Diclofenac Potassium BP/USP 50 mg Rapid Anti-Inflammatory Caffeine Anhydrous BP/USP 30 mg Adjuvant / Vasoconstrictor Excipients Q.S. Microcrystalline Cellulose / HPMC Paroxetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Polymeric Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the extended-release hydrogel network.
Active Ingredient Strength Primary Clinical Function Paroxetine (as HCl Hemihydrate) Ph.Eur./USP 12.5 mg (CR) Initiation Standard: Base titration unit to safely acclimatize the brain and minimize initial side effects. Gold standard for PMDD. Paroxetine (as HCl Hemihydrate) Ph.Eur./USP 25 mg (CR) Global Clinical Standard: Standard adult maintenance dose for Major Depressive Disorder and Severe Panic Disorder. Paroxetine (as HCl Hemihydrate) Ph.Eur./USP 37.5 mg (CR) Advanced Psychiatric Standard: High-dose maintenance therapy for treatment-resistant depression and refractory anxiety. Excipients Hypromellose (HPMC) / Methacrylic Acid Copolymer / Lactose Monohydrate / Magnesium Stearate / Triethyl Citrate Hydrophilic SR Polymer Matrix / Enteric Coating / Diluent / Plasticizer (Engineered to absolutely block stomach acid and control the exact 24-hour intestinal diffusion rate) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic psychiatric dispensing regimens).
Pazopanib Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, High-Density Film-Coated Tablet, packed exclusively in highly secure, child-resistant heavy-gauge HDPE bottles or specialized Alu-Alu blister strips to ensure the absolute chemical stability of the cytotoxic molecule and prevent accidental exposure.
Active Ingredient Strength Primary Clinical Function Pazopanib HCl INN/Ph.Eur. 200 mg (Base Equivalent) Dose-Modification Standard: Essential unit for precise dose reduction in patients experiencing severe hepatic toxicity or adverse drug reactions. Pazopanib HCl INN/Ph.Eur. 400 mg (Base Equivalent) Global Clinical Standard: Primary therapeutic unit designed to achieve the massive 800 mg daily protocol with minimal pill burden. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K30 / Magnesium Stearate / Hypromellose / Titanium Dioxide Diluent / Superdisintegrant / Binder / Lubricant / Premium Cytotoxic-Barrier Film-Coating (Engineered specifically to seal the lethal HPAPI inside the tablet, completely protecting healthcare workers and caregivers from highly toxic dust exposure) *Pack Sizes: Bottles of 30 or 60 Tablets (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
