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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 ,Paracetamol & Trypsin-Chymotrypsin 150000AU Tablets
FreeProduct Composition & Strength
We supply this product as a Film-Coated, Enteric-Shielded Tablet to ensure the enzymes are protected from stomach acid and absorbed in the intestine.
Active Ingredient Strength Primary Clinical Function Aceclofenac USP/BP 100 mg The Anti-Inflammatory: Reduces joint pain and physical swelling of the tissues. Paracetamol USP/BP 325 mg The Analgesic: Provides rapid relief from acute pain and manages fever. Trypsin-Chymotrypsin 150,000 AU The Enzyme Payload: Resolves inflammation and clears edema to accelerate tissue repair. Aceclofenac , Paracetamol and Serratiopeptidase Tablets
FreeProduct Composition & Strength
We supply this product as a Film-Coated, Enteric-Shielded Tablet to ensure the enzyme remains active through the stomach acid.
Active Ingredient Strength Primary Clinical Function Aceclofenac USP/BP 100 mg The Anti-Inflammatory: Reduces joint and tissue inflammation and stiffness. Paracetamol USP/BP 325 mg The Analgesic: Provides rapid relief from acute pain and manages fever. Serratiopeptidase 15 mg The Enzyme Payload: Resolves inflammation and clears edema to accelerate tissue repair. Aceclofenac , Paracetamol and Tizanidine Tablets
FreeProduct Composition & Strength
We supply this product as a Film-Coated Tablet, engineered for synchronized absorption to ensure the muscle relaxant and pain reliever reach therapeutic levels at the same time.
Active Ingredient Strength Primary Clinical Function Aceclofenac USP/BP 100 mg The Anti-Inflammatory: Reduces joint and tissue inflammation and stiffness. Paracetamol USP/BP 325 mg The Analgesic: Provides rapid relief from acute pain and manages fever. Tizanidine (as HCl) USP/BP 2 mg The Muscle Relaxant: Relieves painful muscle spasms and improves physical mobility. 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, Paracetamol & Chlorzoxazone Tablets
FreeProduct Composition & Strength
We supply this product as a Film-Coated Tablet, engineered for synchronized absorption to ensure the muscle relaxant and pain reliever reach therapeutic levels at the same time.
Active Ingredient Strength Primary Clinical Function Aceclofenac USP/BP 100 mg The Anti-Inflammatory: Reduces joint and tissue inflammation and stiffness. Paracetamol USP/BP 325 mg The Analgesic: Provides rapid relief from acute pain and manages fever. Chlorzoxazone USP/BP 250 mg / 500 mg The Muscle Relaxant: Relieves painful muscle spasms and improves physical mobility. Aciclovir Tablets
FreeProduct Composition & Strength
We supply this product in standardized strengths to cover everything from simple cold sores to severe shingles cases.
Active Ingredient Strength Primary Clinical Function Aciclovir USP/BP/Ph.Eur. 200 mg The Herpes Unit: Standard dose for the treatment and suppression of Herpes Simplex (HSV-1 and HSV-2). Aciclovir USP/BP/Ph.Eur. 400 mg The Prophylactic Anchor: Used for long-term suppression in immunocompromised patients. Aciclovir USP/BP/Ph.Eur. 800 mg The Zoster Payload: High-potency dose required to treat Shingles (Herpes Zoster) and Chickenpox. Acitretin Tablets
FreeProduct Composition & Strength
We supply this product in standardized strengths to allow for precise clinical titration, packed in high-barrier Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Acitretin USP/Ph.Eur. 10 mg The Titration Unit: Used to start therapy or for maintenance in patients sensitive to retinoids. Acitretin USP/Ph.Eur. 25 mg The Therapeutic Anchor: The standard dose for achieving rapid clearance of severe skin lesions. Excipients Proprietary Matrix Bio-Stable System: Engineered to ensure consistent oral absorption (approx. 60% bioavailability when taken with food). 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 Adefovir Dipivoxil Tablets
FreeProduct Composition & Strengths
We supply this therapeutic in the globally accepted standard therapeutic strength optimized for adult daily maintenance therapy.
Active Ingredient Standard Strength Primary Clinical Target Adefovir Dipivoxil IP / BP / USP 10 mg The Polymerase Blocker: Daily oral dose to suppress chronic Hepatitis B viral loads. Excipients Pharma Grade The Matrix: High-stability lactose/microcrystalline cellulose binders. 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 Afatinib Tablets
FreeProduct Composition & Strength
We supply this product in multiple strengths to allow for precise dose titration based on patient tolerability.
Active Ingredient Strength Primary Clinical Function Afatinib (as Dimaleate) USP/Ph.Eur. 20 mg / 30 mg The Dose-Adjustment Unit: Used for patients requiring a lower dose due to gastrointestinal or skin toxicity. Afatinib (as Dimaleate) USP/Ph.Eur. 40 mg The Standard Therapeutic Anchor: The globally validated starting dose for first-line treatment of EGFR+ NSCLC. Excipients Proprietary Matrix Bio-Stable Coating: Engineered to protect the sensitive dimaleate salt and ensure consistent systemic absorption. 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 Alfuzosin & Dutasteride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer or Capsule-in-Tablet format, packed in high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive Dutasteride.
Active Ingredient Strength Primary Clinical Function Alfuzosin HCl (Extended-Release) USP/BP 10 mg The Rapid Reliever: Provides immediate improvement in urine flow by relaxing prostate muscles. Dutasteride USP/BP 0.5 mg The Long-Term Shaper: Reduces the physical size of the prostate to prevent the need for surgery. Excipients Hydrophilic Matrix Controlled-Release System: Engineered to provide synchronized 24-hour therapeutic coverage with once-daily dosing. Alfuzosin Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extended-Release (ER) Tablet, packed in high-barrier Alu-Alu blister strips to ensure API stability.
Active Ingredient Strength Primary Clinical Function Alfuzosin Hydrochloride USP/BP 10 mg The Standard Therapeutic Anchor: The globally validated once-daily dose for moderate-to-severe BPH symptoms. Excipients Extended-Release Matrix Controlled-Delivery System: Engineered to provide synchronized 24-hour therapeutic coverage, eliminating the need for multiple daily doses. Alpelisib Tablets
FreeProduct Composition & Strength
We supply this product in standardized daily dose packs, designed to achieve the 300 mg daily therapeutic target.
Active Ingredient Strength Primary Clinical Function Alpelisib USP/Ph.Eur. 50 mg / 150 mg The Combination Unit: Used together (150mg x 2) to reach the standard 300mg daily dose. Alpelisib USP/Ph.Eur. 200 mg The Dose-Reduction Unit: Used for patients requiring a lower dose due to side effects (Hyperglycemia/Rash). Excipients Proprietary Matrix Bio-Stable Coating: Engineered to protect the sensitive API and ensure consistent systemic absorption. Alprostadil Tablets
FreeProduct Composition & Strength
We supply this product in high-purity oral and specialized dispersible formats, primarily for hospital and specialist use.
Active Ingredient Strength Primary Clinical Function Alprostadil USP/BP/Ph.Eur. 0.5 mg The Neonatal Unit: Used in controlled hospital settings for maintaining ductal patency in infants with congenital heart defects. Alprostadil USP/BP/Ph.Eur. 1 mg The Vascular/Urology Anchor: Used for severe peripheral vascular disease or refractory erectile dysfunction. Excipients Proprietary Matrix Bio-Stable System: Engineered to prevent the rapid degradation of the sensitive prostaglandin molecule during transit. 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.
Amantadine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Tablet, packed in moisture-resistant Alu-Alu or Alu-PVC blister strips.
Active Ingredient Strength Primary Clinical Function Amantadine Hydrochloride USP/BP 100 mg The Standard Therapeutic Anchor: The globally validated dose for both Parkinsonian motor control and antiviral prophylaxis. Excipients Proprietary Matrix Rapid-Release System: Engineered to ensure a consistent $T_{max}$ (peak concentration) of approx. 2 to 4 hours for reliable daily protection. Ambrisentan Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Potency Tablet, packed in high-barrier Alu-Alu blister strips to ensure API stability.
Active Ingredient Strength Primary Clinical Function Ambrisentan USP/Ph.Eur. 5 mg The Initiation Unit: The standard starting dose for adults to establish tolerance and initial pulmonary dilation. Ambrisentan USP/Ph.Eur. 10 mg The Maximum Maintenance Payload: For patients requiring additional symptomatic improvement after the 5 mg dose. Excipients Proprietary Matrix Bio-Optimized System: Engineered to ensure a consistent $T_{max}$ (peak concentration) of approx. 2 hours for reliable daily protection. 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. Amlodipine & Enalapril Maleate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets to protect the Enalapril Maleate from moisture-induced degradation and to ensure the physical integrity of the combination.
Active Ingredient Strength (Standard) Therapeutic Role Amlodipine (as Besylate) BP/USP 5 mg / 10 mg Calcium Channel Blocker (CCB) Enalapril Maleate BP/USP 5 mg / 10 mg / 20 mg ACE Inhibitor Excipients Q.S. Sodium Stearyl Fumarate / Lactose Lubricant & Stabilizer Amlodipine Besylate & Losartan Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The formulation is optimized for 24-hour efficacy, allowing for convenient once-daily dosing.
Active Ingredient Strength (Standard) Therapeutic Role Amlodipine Besylate BP/USP 5 mg Calcium Channel Blocker (CCB) Losartan Potassium BP/USP 50 mg Angiotensin Receptor Blocker (ARB) Excipients Q.S. Microcrystalline Cellulose / Starch Stabilizing Core Matrix Amlodipine With Lisinopril Dehydrate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The use of Lisinopril in its Dihydrate form ensures superior stability and predictable dissolution profiles.
Active Ingredient Strength (Standard) Therapeutic Role Amlodipine (as Besylate) BP/USP 5 mg / 10 mg Calcium Channel Blocker Lisinopril (as Dihydrate) BP/USP 5 mg / 10 mg / 20 mg ACE Inhibitor Excipients Q.S. Calcium Phosphate / Mannitol Stabilizing Agents 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 Anastrozole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Cytotoxic Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Anastrozole USP/Ph.Eur. 1 mg The Standard Oncology Anchor: The globally validated dose for both adjuvant and first-line treatment of advanced breast cancer. Excipients Proprietary Matrix High-Containment Coating: Engineered with an impenetrable film-coat to prevent the release of cytotoxic dust, ensuring safety for healthcare workers. Apixaban Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Apixaban USP/Ph.Eur. 2.5 mg The Dose-Reduction Unit: Used for patients with specific risk factors (Age ≥80, Weight ≤60kg, or high Creatinine) to minimize bleeding. Apixaban USP/Ph.Eur. 5 mg The Therapeutic Anchor: The standard maintenance dose for stroke prevention in Atrial Fibrillation and DVT treatment. Excipients Proprietary Matrix Rapid-Dissolution System: Engineered to ensure a consistent $T_{max}$ of approx. 3 to 4 hours for reliable protection. Apremilast tablets
FreeProduct Composition & Strength
We supply this product in a standardized titration pack format or individual strengths to ensure patient safety during the initial phase.
Active Ingredient Strength Primary Clinical Function Apremilast USP/Ph.Eur. 10 mg / 20 mg The Titration Unit: Used during the first 5 days of therapy to minimize gastrointestinal side effects. Apremilast USP/Ph.Eur. 30 mg The Therapeutic Anchor: The standard maintenance dose for long-term control of Psoriasis and Psoriatic Arthritis. Excipients Proprietary Matrix Bio-Synchronized Release: Engineered to ensure a consistent $T_{max}$ of approx. 2.5 hours for steady-state immune modulation. 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 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.
Atazanavir & Ritonavir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, engineered for synchronized 24-hour viral suppression.
Active Ingredient Strength Primary Clinical Function Atazanavir (as Sulfate) USP/BP 300 mg The Antiviral Anchor: Blocks the maturation of HIV, preventing the spread of infection to CD4 cells. Ritonavir USP/BP 100 mg The Pharmacokinetic Booster: Inhibits liver metabolism to maintain high Atazanavir levels for 24 hours. Excipients Proprietary Matrix Bio-Enhancement System: Engineered to ensure maximum intestinal absorption, which is critical for PI-class medications. 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 & Chlorthalidone Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The combination is engineered to maintain therapeutic plasma levels over a 24-hour period, supporting once-daily dosing.
Active Ingredient Strength (Standard) Therapeutic Role Atenolol BP/USP 50 mg / 100 mg Cardioselective Beta-Blocker Chlorthalidone BP/USP 12.5 mg / 25 mg Long-acting Diuretic Excipients Q.S. Magnesium Stearate / Povidone Stabilizing Core Matrix 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.
Azilsartan Medoxomil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in moisture-resistant Alu-Alu blister strips to ensure the stability of the Medoxomil ester.
Active Ingredient Strength Primary Clinical Function Azilsartan Medoxomil Potassium 40 mg The Standard Initiation Unit: The primary starting dose for most adult patients with hypertension. Azilsartan Medoxomil Potassium 80 mg The High-Potency Payload: For patients requiring additional blood pressure lowering beyond the 40 mg dose. Excipients Proprietary Matrix Hydrolysis-Stable System: Engineered to prevent premature breakdown of the prodrug before it reaches the gastrointestinal tract. Baclofen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Disintegration Tablet, packed in moisture-resistant Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Baclofen USP/BP/Ph.Eur. 10 mg The Standard Titration Unit: The primary dose used for gradual escalation to determine patient tolerance and efficacy. Baclofen USP/BP/Ph.Eur. 20 mg The Maintenance Payload: High-potency dose for patients with severe spasticity from chronic spinal cord injuries. Excipients Proprietary Matrix Rapid-Release System: Engineered to ensure a predictable $T_{max}$ (time to peak concentration) of 1 to 2 hours for fast relief. Baricitinib Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Baricitinib USP/Ph.Eur. 2 mg The Standard RA Anchor: The primary maintenance dose for adult patients with moderate-to-severe Rheumatoid Arthritis. Baricitinib USP/Ph.Eur. 4 mg The Dermatology/Severe Payload: High-potency dose utilized for Alopecia Areata and severe Atopic Dermatitis protocols. Excipients Proprietary Matrix Bio-Synchronized System: Engineered to ensure a consistent pharmacokinetic profile (Tmax of approx. 1 hour) for predictable immune suppression. Betahistine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Disintegration Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the active dihydrochloride salt.
Active Ingredient Strength Primary Clinical Function Betahistine Dihydrochloride USP/Ph.Eur. 8 mg / 16 mg The Standard Maintenance Anchor: Ideal for long-term management of vertigo and tinnitus. Betahistine Dihydrochloride USP/Ph.Eur. 24 mg / 48 mg The Therapeutic Payload: High-potency dose for acute phases of Meniere’s Disease and severe vestibular dysfunction. Excipients Proprietary Matrix Gastric-Gentle System: Engineered to ensure rapid absorption while minimizing the common “histamine-like” gastric irritation. Bethanecol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in secure Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Bethanechol Chloride USP/BP 10 mg The Pediatric & Titration Unit: Ideal for initial dosing or mild cases of gastric atony. Bethanechol Chloride USP/BP 25 mg The Urology Anchor: The standardized therapeutic dose for managing post-operative urinary retention. Excipients Proprietary Matrix Acid-Stable Formulation: Engineered to survive the gastric environment for consistent intestinal absorption. Bicalutamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Cytotoxic Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Bicalutamide USP/Ph.Eur. 50 mg The Metastatic Anchor: Used in combination with a LHRH analogue (medical castration) for advanced metastatic disease. Bicalutamide USP/Ph.Eur. 150 mg The Monotherapy Payload: Utilized as a standalone treatment for locally advanced, non-metastatic prostate cancer. Excipients Proprietary Matrix High-Containment Coating: Engineered with an impenetrable film-coat to prevent the release of cytotoxic dust during handling by healthcare professionals. 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 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.
Bosentan Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in moisture-resistant Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Bosentan (as Monohydrate) USP/Ph.Eur. 62.5 mg The Initiation Unit: Utilized for the first 4 weeks of therapy to assess patient tolerance and liver response. Bosentan (as Monohydrate) USP/Ph.Eur. 125 mg The Maintenance Payload: The standardized therapeutic dose for long-term management of PAH and exercise capacity improvement. Excipients Proprietary Matrix Controlled Disintegration System: Engineered to ensure a predictable pharmacokinetic profile, matching the innovator brand’s $T_{max}$ (time to peak concentration). Bromhexine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Disintegration Tablet, packed in moisture-resistant Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Bromhexine Hydrochloride BP/USP 8 mg The Respiratory Anchor: The standardized therapeutic unit for adults and children over 12 for the treatment of productive cough. Excipients Proprietary Matrix Rapid Dissolution System: Engineered to ensure the tablet shatters instantly in the stomach for rapid systemic absorption and lung-tissue penetration. Buclizine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Fast-Acting Tablet, packed in high-barrier Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Buclizine Hydrochloride BP/USP 25 mg The Universal Anchor: The standardized therapeutic unit for both appetite stimulation (adults/pediatrics) and motion sickness prevention. Excipients Proprietary Matrix High-Disintegration System: Engineered to ensure the tablet dissolves rapidly in the gastric environment for a fast onset of action (typically within 30–60 minutes). 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 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.
Canagliflozin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Stability Tablet, packed in secure, moisture-resistant Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Canagliflozin (Hemi-hydrate) USP 100 mg The Metabolic Anchor: Standard starting dose for glycemic control and cardio-renal protection. Canagliflozin (Hemi-hydrate) USP 300 mg The High-Efficacy Payload: Utilized for patients requiring maximal HbA1c reduction with preserved renal function. Excipients Proprietary Matrix Lactose-Optimized Blend: Engineered to ensure rapid disintegration and 100% bioequivalence to the innovator brand. Capecitabine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Cytotoxic Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Capecitabine USP/Ph.Eur. 150 mg The Precision Titration Anchor: Utilized for accurate dose adjustments based on Body Surface Area (BSA). Capecitabine USP/Ph.Eur. 500 mg The Oncology Macrodose: The primary therapeutic unit for standard cycles in Colorectal and Breast cancer. Excipients Proprietary Matrix High-Containment Coating: Engineered with an impenetrable film-coat to prevent the release of cytotoxic dust during handling by healthcare professionals. 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.
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.
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).
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 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).
Chlorpheniramine Tablets
FreeProduct Composition & Strength
We supply this product in the globally accepted standard strength for adult dosing, ensuring safe and effective treatment cycles.
Active Ingredient Strength (per Tablet) Primary Clinical Function Chlorpheniramine Maleate IP/BP/USP 4 mg The H1 Blocker: Rapidly controls acute allergic flares. Excipients Pharma Grade The Matrix: Ensures shelf-life stability and rapid dissolution. 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).
Chymotrypsin Tablets
FreeProduct Composition & Enzyme Potency
We supply this product as a synergistic Trypsin-Chymotrypsin Fixed-Dose Combination (FDC), calibrated in Armour Units (AU) for maximum biological activity.
Active Ingredient Mixture Enzyme Ratio Standard Potency Options Primary Clinical Function Trypsin & Chymotrypsin IP/BP/USP 6:1 50,000 Armour Units (AU) Maintenance Recovery: For standard soft-tissue trauma and mild post-operative edema. Trypsin & Chymotrypsin IP/BP/USP 6:1 100,000 Armour Units (AU) High-Intensity Therapy: For major orthopedic adjustments, dental extractions, and large hematomas. 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). 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).
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 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).
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).
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
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).
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).
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).
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).
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).
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).
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.
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.
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.
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.
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.
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.
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).
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).
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).
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).
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 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 Aluminium Hydroxide, Magnesium Hydroxide & Simethicone Tablets
FreeProduct Composition & Strength
We supply this product as Chewable Tablets, which is the optimal delivery format to ensure the active ingredients are finely dispersed before reaching the stomach.
Active Ingredient Strength Primary Clinical Function Dried Aluminium Hydroxide Gel 250 mg / 300 mg The Sustained Buffer: Provides long-lasting acid neutralization and forms a protective coating on the stomach lining. Magnesium Hydroxide 250 mg The Rapid Neutralizer: Provides immediate relief from heartburn and balances the digestive transit time. Simethicone 25 mg / 50 mg The Defoaming Agent: Physically breaks down gas bubbles to relieve bloating and abdominal discomfort. Flavors Mint / Fruit / Orange Palatability Matrix: Engineered to be pleasant-tasting to ensure high patient compliance for OTC use. 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.
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
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).
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).
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).
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).
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.
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. 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).
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.
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).
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).
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).
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.
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
FreeThe term Fluoxetine Capsules most commonly refers to Fluoxetine Capsules 20 Capsule, a prescription antidepressant.
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).
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).
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 & Metformin Hydrochloride Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) designed for flexible clinical titration.
Active Ingredient Standard Strengths (per Tablet) Primary Clinical Function Metformin HCl 400 mg / 500 mg The Foundation: Reduces glucose production. Glibenclamide (Glyburide) 2.5 mg / 5 mg The Stimulator: Enhances insulin secretion. Excipients Pharma Grade The Matrix: Ensures stability of the FDC. 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).
Glimepiride & Metformin Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Bilayered Tablets or Film Coated Tablets. The bilayered technology is often used to manage the different release profiles and physical characteristics of the two APIs.
Active Ingredient Strength (Standard) Therapeutic Role Glimepiride USP/BP/IP 1 mg / 2 mg Sulfonylurea (Insulin Secretagogue) Metformin HCl USP/BP/IP 500 mg / 1000 mg Biguanide (Insulin Sensitizer) Excipients Q.S. Povidone / Magnesium Stearate Stabilizing Core Matrix Glimepiride, Pioglitazone & Metformin Hydrochloride Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) designed for flexible clinical titration.
Active Ingredient Common Strength Primary Clinical Function Metformin HCl (SR/IR) 500 mg / 1000 mg The Foundation: Reduces glucose production. Glimepiride 1 mg / 2 mg The Stimulator: Enhances insulin secretion. Pioglitazone 15 mg The Sensitizer: Fixes insulin resistance. 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).
Glucose Infusion 10%
FreeActive IngredientStrength (per 100 ml)Primary Clinical FunctionGlucose (Dextrose) IP/BP/USP10.0 gThe Fuel: Provides 34 kcal per 100 ml.ExcipientsWater for Injection (WFI)The Vehicle: Sterile and pyrogen-free.Osmolarity~505 mOsm/LThe Physics: Hypertonic solution.pH Range3.5 to 6.5The Stability: Chemically optimized for shelf-life.
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.
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.
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).
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
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 & Pyridoxine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The ratio of Isoniazid to Pyridoxine is carefully calibrated to meet international clinical guidelines for neuroprotection.
Active Ingredient Strength (Standard) Therapeutic Role Isoniazid BP/USP 300 mg Primary Antitubercular (Bactericidal) Pyridoxine Hydrochloride BP/USP 10 mg / 25 mg / 50 mg Neuroprotective Vitamin (B6) Excipients Q.S. Starch / Lactose / Magnesium Stearate Tablet Core Matrix Isoniazid & Pyridoxine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The ratio of Isoniazid to Pyridoxine is carefully calibrated to meet international clinical guidelines for neuroprotection.
Active Ingredient Strength (Standard) Therapeutic Role Isoniazid BP/USP 300 mg Primary Antitubercular (Bactericidal) Pyridoxine Hydrochloride BP/USP 10 mg / 25 mg / 50 mg Neuroprotective Vitamin (B6) Excipients Q.S. Starch / Lactose / Magnesium Stearate Tablet Core Matrix Isosorbide Mononitrate Tablets
FreeProduct Composition & Strength
We supply this product as Immediate Release Tablets (20 mg). We also offer Extended Release (ER/SR) variants for once-daily dosing through our contract manufacturing division.
Active Ingredient Strength (Standard) Therapeutic Role Isosorbide Mononitrate BP/USP 20 mg Organic Nitrate / Vasodilator Excipients Q.S. Microcrystalline Cellulose / Lactose Stabilizing Matrix Isotretinoin Capsules
FreeProduct Composition & Strengths
We supply this product as Liquid-Filled Soft Gelatin Capsules, optimized for maximum systemic absorption.
Active Ingredient Strength (per Softgel) Primary Clinical Target Isotretinoin IP/BP/USP 10 mg Standard Starting Dose: For mild-to-moderate systemic treatment. Isotretinoin IP/BP/USP 20 mg Therapeutic Dose: For severe, cystic, or conglobate acne. Excipients Soybean Oil / Beeswax The Vehicle: Ensures lipid-solubility for better absorption. 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).
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).
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.
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-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 tablets
FreeProduct Composition & Strength
We supply this product in the internationally standardized Fixed-Dose Combination (FDC) required for therapeutic compliance.
Active Ingredient Strength (per Tablet) Primary Clinical Function Lamivudine (3TC) IP/BP/USP 150 mg The Chain Terminator: High potency, low toxicity. Zidovudine (AZT) IP/BP/USP 300 mg The Foundation: Proven efficacy in preventing replication. Excipients Pharma Grade The Matrix: Ensures stability of the sensitive FDC. Lamivudine Tablets
FreeProduct Composition & Available Portfolio strengths
We manufacture Lamivudine across the precise compendial strengths mandated to manage either targeted chronic hepatic monotherapy or high-potency systemic combination antiretroviral protocols.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Lamivudine USP / BP / IP 100 mg Oral Solid Film-Coated Tablet Chronic Hepatitis B (HBV): Low-dose configuration optimized for standalone daily suppression of active hepatic viral replication. Lamivudine USP / BP / IP 150 mg Oral Solid Film-Coated Tablet Standard Antiretroviral (HIV): Baseline strength designed for twice-daily co-administration or integration into standard multi-drug ARV regimens. Lamivudine USP / BP / IP 300 mg Oral High-Potency Solid Tablet High-Compliance Antiretroviral (HIV): Standard adult once-daily high-dose format engineered to optimize long-term patient compliance. 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).
Leflunomide Tablets
FreeProduct Composition & Available Portfolio Strengths
We supply Leflunomide across the complete compendial strength matrix, enabling clinicians to manage both rapid initial loading cycles and long-term low-dose maintenance blocks.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Leflunomide USP / BP / IP 10 mg Oral Solid Film-Coated Tablet Low-Dose Maintenance: Calibrated for mild-to-moderate maintenance blocks or patients exhibiting sensitive hepatic profiles. Leflunomide USP / BP / IP 20 mg Oral Solid Film-Coated Tablet The Core Commercial Volume: First-line international standard daily maintenance dose for active Rheumatoid and Psoriatic Arthritis. Leflunomide USP / BP / IP 100 mg Oral High-Mass Solid Tablet Initial Loading Regimen: High-potency format utilized exclusively for the rapid 3-day initial tissue saturation phase. 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).
Levamisole Tablets
FreeProduct Composition & Available Strengths
We supply Levamisole Hydrochloride across the two primary compendial configurations required to execute precise pediatric deworming courses or adult high-mass therapeutic maintenance.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Levamisole Hydrochloride USP / BP / IP 50 mg Oral Solid Uncoated / Chewable Tablet Pediatric Deworming & Titration: Low-dose format calibrated for exact mass titration in pediatric ascariasis or low-dose immunomodulatory courses. Levamisole Hydrochloride USP / BP / IP 150 mg Oral Solid Compressed Tablet The Core Commercial Volume: High-potency, single-dose adult baseline format optimized for rapid mass community deworming campaigns. 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.
Levocetirizine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The small, easy-to-swallow tablets are engineered for rapid disintegration to facilitate quick relief from acute allergic flares.
Active Ingredient Strength (Standard) Therapeutic Role Levocetirizine Dihydrochloride BP/USP 5 mg Potent H1-Receptor Antagonist Excipients Q.S. Microcrystalline Cellulose / Lactose Diluent & Disintegrant Coating Agent Q.S. Opadry® White Protective Film Coating 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).
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).
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
Loperamide Tablet
FreeProduct Composition & Configuration
We supply Loperamide Hydrochloride in the internationally standardized 2 mg therapeutic dosage configuration, engineered for rapid disintegration and fast symptomatic relief.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Application Loperamide Hydrochloride USP / BP / IP 2 mg Oral Solid Immediate-Release Uncoated Tablet Fast-Acting Anti-Diarrheal: Non-specific acute diarrhea management, chronic diarrheal stabilization, and ileostomy output reduction. Excipients Pharma Grade Lactose Monohydrate, Microcrystalline Cellulose, Corn Starch, Magnesium Stearate The Disintegration Scaffold: Optimized matrix for high mechanical stability and rapid water wicking. 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 Loratidine Tablet
FreeProduct Composition & Available Strengths
We supply Loratadine in the internationally recognized 10 mg therapeutic dosage configuration, optimized for maximum daily compliance and clean absorption kinetics.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Application Loratadine USP / BP / IP 10 mg Oral Solid Immediate-Release Uncoated Tablet 24-Hour Allergy Control: Treatment of allergic rhinitis (hay fever), chronic idiopathic urticaria (hives), and ocular allergic reactions. Excipients Pharma Grade Lactose Monohydrate, Corn Starch, Magnesium Stearate The Disintegration Scaffold: Optimized matrix for high mechanical stability during bulk shipping and rapid water-wicking in the gut. 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 Losartan Tablet
FreeProduct Composition & Available Strengths
We supply Losartan Potassium across the complete, internationally recognized therapeutic range to facilitate progressive dose titrations and precise maintenance regimens.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Losartan Potassium USP / BP / IP 25 mg Oral Solid Film-Coated Tablet Pediatric & Low-Dose Titration: For introductory pediatric hypertension care or initial combination-therapy building. Losartan Potassium USP / BP / IP 50 mg Oral Solid Film-Coated Tablet Core Commercial Volume: Standard international baseline daily dose for mild-to-moderate chronic essential hypertension. Losartan Potassium USP / BP / IP 100 mg Oral High-Potency Solid Tablet Maximal Saturation Maintenance: For advanced hypertensive management, diabetic nephropathy progression delay, and stroke risk reduction in left ventricular hypertrophy. 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.
Mebendazole Tablet
FreeProduct Composition & Available Formats
We supply Mebendazole across the two primary compendial configurations required to execute either targeted individual eradication or high-velocity single-dose mass eradication protocols.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Mebendazole USP / BP / IP 100 mg Oral Solid Chewable / Dispersible Tablet Targeted Multi-Dose Therapy: Standard baseline format for individual 3-day courses targeting specific multi-worm infestations (Pinworms, Roundworms, Hookworms). Mebendazole USP / BP / IP 500 mg High-Mass Oral Solid Single-Dose Tablet Mass Public Health Eradication: High-potency, single-dose format engineered for rapid deployment in mass community deworming campaigns. Mebeverine Tablet
FreeProduct Composition & Available Formats
We supply Mebeverine Hydrochloride in both rapid-acting immediate-release and advanced continuous-release configurations to accommodate customized patient compliance tracking.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Mebeverine Hydrochloride IP / BP / USP 135 mg Oral Solid Immediate-Release Film-Coated Tablet Targeted Acute Dosing: Fast-acting formulation designed for standard three-times-daily administration prior to localized food triggers. Mebeverine Hydrochloride IP / BP / USP 200 mg SR Sustained-Release Hydrophilic Polymer Matrix Tablet / Capsule Continuous 24-Hour Coverage: Premium, once- or twice-daily formulation engineered to release active molecules continuously, eliminating nocturnal spikes and maximizing compliance. 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).
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 Tablet
FreeProduct Composition & Portfolio Range
We manufacture Metformin SR in the full spectrum of internationally recognized therapeutic strengths, utilizing a specialized slow-release scaffold to reduce dosing frequency to once daily.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Metformin Hydrochloride IP / BP / USP 500 mg Hydrophilic Dual-Polymer Sustained-Release Initial Titration: For low-dose introductory management and early-stage Type 2 stabilization. Metformin Hydrochloride IP / BP / USP 750 mg Hydrophilic Dual-Polymer Sustained-Release Intermediate Scaling: Step-up strength to optimize glycemic indices without increasing tablet count. Metformin Hydrochloride IP / BP / USP 1000 mg Hydrophilic Dual-Polymer Sustained-Release High-Potency Maintenance: Maximizes daily therapeutic saturation in an elegant, once-daily single tablet format. Metformin Tablets
FreeProduct Composition & Available Specifications
We supply Metformin Hydrochloride across the full spectrum of compendial strengths and advanced kinetic delivery platforms to optimize patient compliance and reduce gastrointestinal side effects.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Metformin Hydrochloride USP / BP / IP 500 mg Oral Solid Immediate-Release Film-Coated Tablet Introductory Titration: Baseline format designed for low-dose introductory management and gradual step-up scaling. Metformin Hydrochloride USP / BP / IP 850 mg Oral Solid Immediate-Release Film-Coated Tablet High-Density Single Dose: Intermediate strength optimized for achieving target daily therapeutic thresholds with fewer tablets. Metformin Hydrochloride USP / BP / IP 1000 mg Oral High-Mass Immediate-Release Tablet Maximal Saturation Therapy: High-strength configuration calibrated for advanced glycemic control and high-dose combinations. Metformin Hydrochloride USP / BP / IP 500 mg / 1000 mg SR Extended/Sustained-Release Hydrophilic Polymer Matrix Premium GI-Comfort Compliance: Once-daily formulation utilizing a dual-layer hydrogel matrix to release active drug slowly, completely eliminating gastrointestinal distress. 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).
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.
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.
Metoclopramide Tablet
FreeProduct Composition & Packaging Specification
We supply Metoclopramide in the globally standardized therapeutic strength optimized for adult baseline three-times-daily dosage regimens.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Function Metoclopramide Hydrochloride USP / BP / IP 10 mg Oral Solid Uncoated Tablet (Scored for micro-dosing titration) The Prokinetic Driver: Accelerates upper gastrointestinal transit and blocks central emetic signals. Excipients Pharma Grade Lactose, Starch, Magnesium Stearate The Core Scaffold: High-solubility matrix engineered for rapid physical disintegration. 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).
Metoprolol Tablet
FreeCore Product Catalog:
Active Ingredient Monograph Standard Strengths Dosage Format Primary Clinical Target Metoprolol Tartrate IP/BP/USP 25 mg Immediate-Release Solid Tablet Acute Titration: For fine-tuned early adjustment in arrhythmias and mild hypertension. Metoprolol Tartrate IP/BP/USP 50 mg Immediate-Release Solid Tablet Standard Twice-Daily Blockade: Routine maintenance for Angina Pectoris and post-Myocardial Infarction stabilization. Metoprolol Tartrate IP/BP/USP 100 mg Immediate-Release Solid Tablet High-Threshold Control: For refractory tachyarrhythmias and intensive post-MI clinical management. 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 Tablet
FreeProduct Composition & Available Strengths
We supply Metronidazole in standard, internationally recognized strengths optimized for adult and pediatric treatment regimens.
Active Ingredient Available Strengths Common Dosage Matrix Primary Clinical Target Metronidazole BP / IP / USP 200 mg Film-Coated / Uncoated Oral Tablet Pediatric & Low-Dose Titration: For delicate adjustments in mild amoebic dysentery or combination protocols. Metronidazole BP / IP / USP 400 mg Film-Coated / Uncoated Oral Tablet Standard Generic Backbone: Standard twice or thrice-daily dosing for dental abscesses and Giardiasis. Metronidazole BP / IP / USP 500 mg High-Potency Oral Tablet Institutional Target: High-volume strength preferred for anaerobic surgical prophylaxis and severe trichomoniasis. 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).
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).
Misoprostol Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets, often hexagonal or scored, to allow for precise dosing. Due to the high potency of the API, we ensure rigorous content uniformity.
Active Ingredient Strength (Standard) Therapeutic Role Misoprostol BP/USP 200 mcg (0.2 mg) Prostaglandin E1 Analogue Excipients Q.S. Microcrystalline Cellulose / HPMC Stabilizing Dispersion Matrix 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).
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).
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).
Nelfinavir Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. Due to the high dose required for therapeutic efficacy, we ensure the tablet is engineered for ease of swallowing without compromising the structural integrity of the high-API load.
Active Ingredient Strength (Standard) Therapeutic Role Nelfinavir Mesylate USP/BP 250 mg Standard Adult / Pediatric Dose Nelfinavir Mesylate USP/BP 625 mg High-Strength Adult Maintenance Excipients Q.S. Calcium Silicate / Crospovidone Disintegrant & Stabilizer 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).
Nevirapine Tablet
FreeProduct Composition & Strengths
We supply this antiretroviral therapeutic in the globally accepted standard therapeutic strength optimized for adult combination maintenance therapy.
Active Ingredient Standard Strength Formulation Delivery Matrix Primary Clinical Function Nevirapine Anhydrous IP / BP / USP 200 mg Oral Solid Uncoated Tablet (Scored for flexible pediatric/titration dividing) The NNRTI Anchor: Suppresses viral replication loads when used in combination ARV regimens. Excipients Pharma Grade Lactose, Microcrystalline Cellulose, Sodium Starch Glycolate The Delivery Core: Ensures immediate physical disintegration and release kinetics. 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).
Nicoumalone Tablet
FreeProduct Composition & Calibration Spectrum
We manufacture Nicoumalone in a complete, highly precise range of strengths to allow for the exact dosage adjustments required to maintain narrow therapeutic targets.
Active Ingredient Common Name Compendial Monograph Available Strengths Primary Clinical Application Nicoumalone (Acenocoumarol) BP / IP / USP 1 mg Micro-Titration Phase: For delicate, low-dose fine-tuning in geriatric or sensitive patient profiles. Nicoumalone (Acenocoumarol) BP / IP / USP 2 mg Foundational Maintenance: The standard baseline dose for routine daily thromboembolic prophylaxis. Nicoumalone (Acenocoumarol) BP / IP / USP 3 mg Intermediate Control: For patients requiring step-up adjustment to hit targeted coagulation thresholds. Nicoumalone (Acenocoumarol) BP / IP / USP 4 mg High-Threshold Suppression: For rapid oral loading or patients presenting high chemical resistance to standard doses. 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.
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).
Olanzepine Tablet
FreeProduct Composition & Available Strengths
We supply Olanzapine in standard, exact strengths to facilitate initial titration phases and safe daily maintenance therapy.
Active Ingredient Available Strengths Primary Clinical Target Olanzapine IP / BP / USP 2.5 mg Introductory Titration: For low-dose introductory cycles, elderly adjustment, or sensitive patient profiles. Olanzapine IP / BP / USP 5 mg Standard Maintenance: The baseline daily dosage for long-term schizophrenic and bipolar maintenance. Olanzapine IP / BP / USP 10 mg Acute Crisis Control: High-potency therapeutic dosing to stabilize acute manic or severe psychotic episodes. 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.
Ondansetron Orally Disintegrating Tablets
FreeProduct Composition & Available Formats
We supply Ondansetron ODT in the two primary compendial configurations required to support initial introductory pediatric dosing up to high-potency surgical and oncological maintenance regimens.
Active Ingredient Monograph Available Strengths Formulation Delivery Matrix Primary Clinical Application Ondansetron Base / Hydrochloride USP / BP / IP 4 mg Fast-Dispersing Hydrophilic Matrix (ODT) Pediatric & General Antiemetic: First-line baseline dosing for acute gastroenteritis, pediatric oncology protocols, and mild post-operative nausea. Ondansetron Base / Hydrochloride USP / BP / IP 8 mg Fast-Dispersing Hydrophilic Matrix (ODT) High-Potency Emetic Control: Advanced strength engineered for highly emetogenic chemotherapy cycles, abdominal radiation protocols, and immediate post-surgical recovery fields. Ondansetron Tablet
FreeProduct Composition & Available Strengths
We supply this critical supportive therapeutic in standard, internationally recognized strengths designed for exact preventative and rescue dosing.
Active Ingredient Available Strengths Primary Clinical Target Ondansetron HCl IP / BP / USP 4 mg Standard Prophylaxis: For moderate emetogenic chemotherapy, general post-operative rescue, and pediatric care. Ondansetron HCl IP / BP / USP 8 mg High-Potency Protection: For highly emetogenic cisplatin-based cancer regimens and severe surgical recovery. 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).
ORS – Oral Rehydration Salt
FreeOral Rehydration Salts IP
Each 4.2 gm contains :
Sodium Chloride IP 0.52 gm
Potassium Chloride IP 0.30 gm
Sodium Citrate IP 0.58 gm
Anhydrous Glucose IP 2.70 gm
Excipients qs
Refreshing FlavourOral Rehydration Salts IP
Each 21 gm contains :
Sodium Chloride IP 2.6 gm
Potassium Chloride IP 1.5 gm
Sodium Citrate IP 2.9 gm
Anhydrous Dextrose IP 13.5 gm
Excipients qs
Refreshing Orange FlavourOral Rehydration Salts BP
Each 4.2 gm contains :
Sodium Chloride BP 0.52 gm
Potassium Chloride BP 0.30 gm
Sodium Citrate BP 0.58 gm
Anhydrous Glucose BP 2.70 gm
Refreshing FlavourOral Rehydration Salts BP
Each 21 gm contains :
Sodium Chloride BP 2.6 gm
Potassium Chloride BP 1.5 gm
Sodium Citrate BP 2.9 gm
Anhydrous Glucose BP 13.5 gm
Refreshing Orange FlavourORASEL / ORAL REHYDRATION SALT B.P. Each 21 gm sachet contains: Anhydrous glucose BP 13.5 g Sodium Chloride BP 2.6 g Sodium citrate BP 2.9 g Potassium Chloride BP 1.5 g Refreshing orange Flavour
HEALTHY ORS /ORAL REHYDRATION SALTS BP EACH 20.5 GM CONTAINS:: – POTASSIUM CHLORIDE BP 1.5 GM
– SODIUM CITRATE BP 2.9 GM
– ANHYDROUS GLUCOSE BP 13.5 GM
– SODIUM CHLORIDE BP BP 2.6 GM – EXCIPIENTS QSUsage: – To replace salts and water that the body loses when you have dehydration caused by gastroenteritis, diarrhea, or vomiting
Category: – Generic Drugs and Medicine
Therapeutic category: – Generic Drugs
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).
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).
Oxcarbazepine Tablet
FreeProduct Composition & Available Strengths
We manufacture Oxcarbazepine in the full, internationally standardized range of strengths to allow for the precise, progressive dose titration mandatory in anti-epileptic therapy.
Active Ingredient Available Strengths Primary Clinical Target Oxcarbazepine IP / BP / USP 150 mg Pediatric & Initial Titration: For low-dose introductory phases to assess patient tolerance. Oxcarbazepine IP / BP / USP 300 mg Standard Maintenance: The foundational daily maintenance dose for adolescent and adult stabilization. Oxcarbazepine IP / BP / USP 600 mg High-Potency Control: For refractory focal seizures or high-threshold therapeutic stabilization. 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).
Pantoprazole Tablets
FreePantoprazole Tablets IP 40 mg
Each Enteric Coated tablet contains
Pantoprazole Sodium IP
Eq. To Pantoprazole 40 mgPenta-20
Pantoprazole Tablets 20 mg
Each Enteric Coated Tablet Contains
Pantoprazole Sodium Sesquihydrate
Eq To Pantoprazole 20 mgPenta – 40
Pantoprazole Tablets 40 mg
Each Entreric Coated tablet contains
Pantoprazole Sodium Sesquihydrate
Eq. To pantoprazole 40 mgUsage: – Heartburn, acid reflux and gastro-esophageal reflux disease
Category: – Antacid & Anti ulcer drugs
Therapeutic category: – Antiulcer, Antacid
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 Caffeine Chlorpheniramine Maleate Phenylephrine Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) optimized for maximum clinical efficacy.
Active Ingredient Strength (per Tablet) Primary Clinical Function Paracetamol (Acetaminophen) 325 mg / 500 mg The Pain & Fever Reliever: Targets aches and chills. Caffeine (Anhydrous) 30 mg The Potentiator: Boosts pain relief and alertness. Chlorpheniramine Maleate 2 mg / 4 mg The Antiallergic: Stops sneezing and runny nose. Phenylephrine HCl 5 mg / 10 mg The Decongestant: Clears blocked sinuses. 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, 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).
Pemetrexed Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Light-Yellow Cake) in glass vials.
Active Ingredient Strength Reconstitution Pemetrexed Disodium 100 mg Requires 0.9% Sodium Chloride Pemetrexed Disodium 500 mg Requires 0.9% Sodium Chloride Pemetrexed Disodium 1000 mg (1 g) High-Dose Protocols Excipients Mannitol / Hydrochloric Acid / Sodium Hydroxide Bulking Agent / pH Adjusters (pH 6.6 – 7.8) *Pack Sizes: Single Vial. (Must be handled with strict cytotoxic precautions).
Pentoxifylline Tablets
FreePentoxifylline Tablets 400 mg
Each Filmcoated tablet contains :
Pentoxifylline BP 400 mgUsage: – To reduce leg pain caused by poor blood circulation
Category: – Anti Cardiovascular drugs
Therapeutic category: – Cardiovascular
Perindopril Erbumine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips equipped with active desiccants to ensure the absolute chemical stability of the highly degradable Erbumine salt.
Active Ingredient Strength Primary Clinical Function Perindopril Erbumine Ph.Eur./USP 2 mg Initiation Standard: Base titration dose for elderly patients or those with severe heart failure/renal impairment to prevent sudden hypotension. Perindopril Erbumine Ph.Eur./USP 4 mg Hypertension Standard: Standard adult maintenance dose for the continuous control of essential hypertension. Perindopril Erbumine Ph.Eur./USP 8 mg Cardiovascular Risk Standard: Maximum maintenance dose for profound risk reduction in patients with stable coronary artery disease. Excipients Microcrystalline Cellulose / Lactose Anhydrous / Hydrophobic Colloidal Silica / Magnesium Stearate Diluent / Alkaline Stabilizer / Moisture Scavenger / Lubricant (Engineered specifically to create a hyper-dry internal tablet matrix that absolutely prevents hydrolytic cyclization of the API) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Phenazopyridine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant PVC/PVDC or Alu-PVC blister strips to ensure the stability of the active dye compound.
Active Ingredient Strength Primary Clinical Function Phenazopyridine Hydrochloride USP/Ph.Eur. 100 mg Standard OTC/Initiation dose for mild-to-moderate urinary tract discomfort. Phenazopyridine Hydrochloride USP/Ph.Eur. 200 mg Global Prescription Standard: Maximum adult dose for severe dysuria and post-operative catheter trauma. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate Diluent / Superdisintegrant (Engineered for rapid gastric dissolution and swift renal clearance) Phenazopyridine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant high-density PVC/PVDC or Alu-PVC blister strips to ensure absolute chemical stability and prevent dye leakage.
Active Ingredient Strength Primary Clinical Function Phenazopyridine HCl USP/Ph.Eur. 100 mg OTC Standard: Base therapeutic unit for mild to moderate UTI symptom relief. Phenazopyridine HCl USP/Ph.Eur. 200 mg Prescription Standard: Maximum adult dose for severe, acute dysuria and post-surgical trauma. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Heavy Carnauba Wax Coating Diluent / Superdisintegrant / Binder / Lubricant / Premium Film-Coating (Engineered specifically to seal the intense red dye inside the tablet, preventing it from staining the patient’s hands or mouth upon swallowing) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-turnover acute dispensing and short-term 2-day urology protocols).
Pheniramine Maleate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Clear Solution in glass ampoules.
Active Ingredient Strength Total Content (2 ml) Pheniramine Maleate BP/USP 22.75 mg / ml 45.5 mg (per 2 ml Ampoule) Excipients Water for Injection Isotonic Solution *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Pioglitazone Tablets
FreePioglitazone Tablets IP 15 mg
Each Uncoated tablet contains :
Pioglitazone Hydrochloride IP
Eq. To Pioglitazone 15 mgPioglitazone Tablets IP 30 mg
Each Uncoated tablet contains :
Pioglitazone Hydrochloride IP
Eq. To Pioglitazone 30 mgPioglitazone With Metformin Tablet
Each Film Coated Tablet contains :
Pioglitazone Hydrochloride IP
Eq. to Pioglitazone 15 mg
Metformin Hydrochloride IP 500 mgUsage: – Type 2 diabetes mellitus
Category: – Anti Diabetic drugs
Therapeutic category: – Anti Diabetic
Piracetam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Clear Solution in glass ampoules or large volume infusion bottles.
Active Ingredient Strength Volume Piracetam BP/USP 200 mg / ml 5 ml Ampoule (1 g Total) Piracetam BP/USP 200 mg / ml 15 ml Ampoule (3 g Total) Piracetam BP/USP 200 mg / ml 60 ml Infusion Bottle (12 g Total) Excipients Sodium Acetate / Acetic Acid Buffer (pH 5.0 – 7.0) *Pack Sizes: Tray of 5/10 Ampoules or Single Infusion Bottle.
Piracetam 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 heavy-gauge PVC/PVDC blister strips to ensure the absolute chemical stability of the highly hygroscopic API.
Active Ingredient Strength Primary Clinical Function Piracetam Ph.Eur./USP 400 mg Initiation / Pediatric Standard: Base unit for pediatric dyslexia and mild vertigo management. Piracetam Ph.Eur./USP 800 mg Global Cognitive Standard: Standard adult maintenance dose for age-related cognitive decline and memory impairment. Piracetam Ph.Eur./USP 1200 mg Acute Neurology Standard: Massive-dose unit designed specifically for Cortical Myoclonus and intensive post-stroke rehabilitation protocols to minimize pill burden. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Macrogol (PEG) / Colloidal Silicon Dioxide / Magnesium Stearate High-Density Diluent / Superdisintegrant / Premium Film-Coating (Engineered specifically to compress the massive API load into a smooth, swallowable, moisture-resistant oblong tablet) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, high-volume chronic neurology dispensing where patients may consume 2.4g to 4.8g daily).
Piroxicam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Pale Yellow to Yellow Aqueous-Solvent Solution in glass ampoules.
Active Ingredient Concentration Total Content & Format Piroxicam USP/BP 20 mg / ml 20 mg in 1 ml Glass Ampoule Piroxicam USP/BP 20 mg / ml 40 mg in 2 ml Glass Ampoule Excipients Propylene Glycol / Benzyl Alcohol Solvent System / Local Anesthetic (Preservative) *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Piroxicam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet or Hard Gelatin Capsule, 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 insoluble active ingredient.
Active Ingredient Strength Primary Clinical Function Piroxicam USP/Ph.Eur. 10 mg Initiation / Elderly Standard: Reduced dose for elderly patients or those with mild renal impairment to mitigate gastrointestinal risks. Piroxicam USP/Ph.Eur. 20 mg Global Clinical Standard: Maximum adult daily dose for the once-daily, continuous suppression of severe rheumatoid and osteoarthritis. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Magnesium Stearate Diluent / Superdisintegrant / Wetting Agent / Lubricant (Engineered specifically with high-grade surfactants to force the rapid gastric dissolution of the highly water-insoluble Piroxicam API) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic rheumatology and orthopedic dispensing regimens).
Pramipexole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly light-sensitive dihydrochloride monohydrate salt.
Active Ingredient Strength Primary Clinical Function Pramipexole (as Dihydrochloride Monohydrate) Ph.Eur./USP 0.125 mg Micro-Dose Standard: Mandatory initiation unit to prevent orthostatic shock, and the gold-standard maintenance dose for RLS. Pramipexole (as Dihydrochloride Monohydrate) Ph.Eur./USP 0.25 mg / 0.5 mg Titration Standard: Mid-level doses for the gradual, safe escalation of Parkinson’s therapy. Pramipexole (as Dihydrochloride Monohydrate) Ph.Eur./USP 1 mg Advanced PD Standard: High-dose maintenance therapy for severe, refractory Parkinson’s Disease. Excipients Mannitol / Maize Starch / Povidone K25 / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered for immediate gastric dissolution and rapid, highly predictable systemic absorption) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict, high-compliance chronic neurology dispensing and complex titration regimens).
Prasugrel Tablet
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 containing dedicated desiccants to ensure the absolute chemical stability of the highly volatile thienopyridine molecule.
Active Ingredient Strength Primary Clinical Function Prasugrel HCl INN/Ph.Eur. 5 mg Dose-Adjusted Standard: Maintenance dose strictly for vulnerable patients weighing < 60 kg or aged ≥ 75 years to minimize fatal bleeding risk. Prasugrel HCl INN/Ph.Eur. 10 mg Global Clinical Standard: Standard adult maintenance dose following a 60 mg acute loading dose in the Cath Lab. Excipients Microcrystalline Cellulose / Mannitol / Croscarmellose Sodium / Hypromellose / Triacetin Diluent / Superdisintegrant / Moisture-Barrier Film-Coating (Engineered specifically to prevent hydrolytic degradation and ensure ultra-fast gastric release) *Pack Sizes: 10×10 Alu-Alu Blisters or 28/30-Tablet Calendar Blisters (Optimized specifically for strict 12-month post-PCI dual-antiplatelet dispensing regimens).
Pregabalin & Methylcobalamin Capsules
FreePregabalin and methylcobalamin capsules are a common combination therapy used to manage neuropathic pain (nerve pain). They are most frequently available in strengths of 75 mg / 750 mcg or 75 mg / 1500 mcg.
Pregabalin & Methylcobalamin 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 to ensure the absolute chemical stability of the highly light-sensitive B12 coenzyme and the SR polymer network.
Active Ingredient Strength Primary Clinical Function Pregabalin INN/Ph.Eur. 75 mg (Sustained-Release) 24-hour controlled suppression of neuropathic pain and hyperalgesia. Methylcobalamin (Mecobalamin) JP/USP 1500 mcg Global Clinical Standard: High-dose active B12 for the anatomical regeneration of the myelin sheath. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Colloidal Silicon Dioxide / Titanium Dioxide / Magnesium Stearate Hydrophilic SR Polymer Matrix / Diluent / Glidant / UV-Blocking Film-Coating (Engineered to control the exact 24-hour diffusion rate while shielding the API from light degradation) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic diabetology and neurology dispensing regimens).
Pregabalin & Nortriptyline 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 absolute chemical stability and to mask the extremely bitter taste of the TCA component.
Active Ingredient Strength Primary Clinical Function Pregabalin INN/Ph.Eur. 50 mg / 75 mg Calcium channel neuromodulation for the direct suppression of hyperactive nerve firing. Nortriptyline Hydrochloride BP/USP 10 mg (Base Equivalent) Global Clinical Standard: SNRI/TCA action to amplify the brain’s natural descending pain-inhibiting pathways. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Titanium Dioxide Diluent / Superdisintegrant / Binder / Premium Film-Coating (Engineered specifically to ensure immediate, synchronized gastric dissolution while completely masking the bitter taste of Nortriptyline) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Pregabalin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Hard Capsule or Extended-Release Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the active amino acid derivative and prevent illicit tampering.
Active Ingredient Strength Primary Clinical Function Pregabalin INN/Ph.Eur. 75 mg Initiation Standard: Base titration unit to safely acclimatize the brain and minimize initial dizziness. Pregabalin INN/Ph.Eur. 150 mg / 300 mg Global Clinical Standard: Advanced maintenance doses for severe diabetic neuropathy, fibromyalgia, and refractory epilepsy. Excipients (Capsules) Pregelatinized Starch / Talc / Hard Gelatin Shell Diluent / Glidant / Capsule Matrix (Engineered for immediate gastric dissolution and rapid systemic onset within 1 hour) *Pack Sizes: 10×10 Alu-Alu Blisters or 14-Capsule Titration Packs (Optimized specifically for strict chronic pain dispensing regimens and controlled-substance tracking).
Prochlorperazine Tablets
FreeProchlorperazine Maleate Tablets IP 5 mg
Each Uncoated Tablet contains :
Prochlorperazine Maleate IP 5 mgUsage: – control severe nausea and vomiting
Category: – Antipsychotic / CNS Drugs
Therapeutic category: – Antipsychotic
Procyclidine 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 hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Procyclidine HCl BP/Ph.Eur. 5 mg Global Clinical Standard: Base therapeutic unit for the rapid reversal of EPS and parkinsonian rigidity. Excipients Lactose Monohydrate / Sodium Starch Glycolate / Povidone / Magnesium Stearate Diluent / Superdisintegrant / Binder / Lubricant (Engineered for rapid gastric dissolution and ultra-fast crossing of the blood-brain barrier) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-volume daily dispensing in acute psychiatric and neurology wards).
Promethazine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Colorless to Faint Yellow Solution in glass ampoules.
Active Ingredient Concentration Total Content & Format Promethazine HCl USP/BP 25 mg / ml 50 mg in 2 ml Glass Ampoule (Standard Dose) Promethazine HCl USP/BP 50 mg / ml 100 mg in 2 ml Glass Ampoule (High Dose) Excipients Disodium Edetate / Sodium Metabisulfite Antioxidant / Preservative System *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Promethazine Tablets
FreePromethazine Hydrochloride Tablets IP 25 mg
Each Sugarcoated tablet contains :
Promethazine Hydrochloride IP 25 mgPromethazine Hydrochloride Tablets BP 10 mg
Each Sugarcoated Tablet Contains:
Promethazine Hydrochloride BP 10 mgPromethazine Hydrochloride Tablets BP
Each Sugarcoated tablet contains :
Promethazine Hydrochloride BP 25 mgUsage: – Treat anaphylaxis
Category: – Anti Allergic drugs
Therapeutic category: – Antihistamine, Anti Allergic, Antiemetic, Anti Vomiting
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
Propanthaline Tablets
FreeXyproline Tablets
Propanthaline Tablets IP 15 mg
Each Coated tablet contains :
Propanthaline Bromide IP 15 mgUsage: – treat ulcers
Category: – Generic Drugs and Medicine
Therapeutic category: – Generic Drugs
Propofol Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, White, Oil-in-Water Emulsion in glass vials or ampoules.
Active Ingredient Concentration Total Content & Format Propofol USP/BP 1% (10 mg / ml) 100 mg in 10 ml Glass Ampoule Propofol USP/BP 1% (10 mg / ml) 200 mg in 20 ml Glass Vial Propofol USP/BP 1% (10 mg / ml) 500 mg in 50 ml Glass Vial (For Infusion) Lipid Vehicle Soybean Oil / Egg Lecithin / Glycerol Macro-emulsion Base (Caloric value: 1.1 kcal/ml) *Pack Sizes: Tray of 5/10 Ampoules or Single Infusion Vials.
Prulifloxacin 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 chemical stability of the ester prodrug.
Active Ingredient Strength Primary Clinical Function Prulifloxacin INN/Ph.Eur. 600 mg Global Clinical Standard: Maximum adult daily dose for the rapid eradication of susceptible UTI and RTI pathogens. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone / Magnesium Stearate / Hypromellose Diluent / Superdisintegrant / Binder / Lubricant / Premium Film-Coating (Engineered for immediate gastric dissolution and synchronized prodrug absorption) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for standard 3-to-10 day acute urology and respiratory infection dispensing regimens).
Pyrazinamide Tablets
FreePyrazinamide Tablet IP
Each Coated Tablets Contains:
Pyrazinamide IP 500 mgPyrazinamide tablet IP 750 mg
Each Coated Tablet Contains:
Pyrazinamide IP 750 mgPYRAZINAMIDE TABLETS BP 400 MG
Each filmcoated tablet contains:
Pyrazinamide BP 400 mgUsage: – Treat tuberculosis (TB)
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic, Antituberculosis
Pyridostigmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-density HDPE bottles with desiccants to ensure the absolute chemical stability of the highly hygroscopic bromide salt.
Active Ingredient Strength Primary Clinical Function Pyridostigmine Bromide USP/Ph.Eur. 60 mg Global Clinical Standard: Base maintenance dose for continuous 24-hour neuromuscular control in MG patients. Excipients Silicone Dioxide / Microcrystalline Cellulose / Pregelatinized Starch / Magnesium Stearate Glidant / Diluent / Binder / Lubricant (Engineered for immediate gastric dissolution and precise, rapid systemic onset within 30-45 minutes) *Pack Sizes: Bottles of 100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-volume daily neurology regimens where patients may consume 6 to 10 tablets daily).
Quinapyramine Sulphate And Quinapyramine Chloride Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials, requiring reconstitution with Sterile Water for Injection to form an aqueous suspension.
Active Ingredient Standard 2.5 g Vial Function Quinapyramine Sulphate BP (Vet) 1.5 g Curative (Immediate Release) Quinapyramine Chloride BP (Vet) 1.0 g Prophylactic (Slow Release / Depot) Total Pro-salt Content 2.5 g *Reconstitute with 15 ml Sterile Water *Pack Sizes: Single 2.5g or 3g Vial, often packed with a Sterile Water diluent ampoule.
Quinine Sulphate Tablets
FreeGlaquine
Quinine Sulphate Tablets BP 300 mg
Eac Sugarcoated tablet contains :
Quinine Sulphate BP 300 mgUsage: – treat malaria caused by mosquito bites
Category: – Antimalarial drugs
Therapeutic category: – Antimalarial
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
Rabeprazole & Domperidone Capsules
FreeRabeprazole and domperidone capsules are a common combination therapy used to treat gastrointestinal disorders where acid reflux is accompanied by nausea or vomiting. They are most frequently available in a fixed-dose strength of 20 mg (enteric-coated) and 30 mg (sustained-release)
Rabeprazole & Levosulpiride Capsules
FreeRabeprazole and levosulpiride capsules are a common combination used to treat gastrointestinal disorders where acid reflux is accompanied by bloating or delayed stomach emptying. They are most frequently available in a fixed-dose strength of 20 mg (enteric-coated) and 75 mg (sustained-release).
Rabeprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Pale Yellow Cake) in clear glass vials.
Active Ingredient Strength Reconstitution Requirement Rabeprazole Sodium USP/BP 20 mg Requires 5 ml of Sterile Water for Injection Excipients Mannitol / Sodium Hydroxide Bulking Agent / Alkalizing Stabilizer *Pack Sizes: Single Vial or Tray of 10 Vials. (Often packed with a 5 ml diluent ampoule).
Rabeprazole Sodium Enteric Coated & Cinitapride Sustained Release Capsules
FreeRabeprazole sodium and cinitapride capsules are a combination therapy used for gastrointestinal disorders where acid reflux co-exists with slow gut movement (dysmotility). They typically come in a fixed-dose strength of 20 mg (enteric-coated) and 3 mg (sustained/extended-release).
Rabeprazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly acid-labile Rabeprazole sodium salt.
Active Ingredient Strength Primary Clinical Function Rabeprazole Sodium INN/Ph.Eur. 10 mg Maintenance Standard: Long-term maintenance of healed erosive esophagitis and symptomatic GERD. Rabeprazole Sodium INN/Ph.Eur. 20 mg Global Clinical Standard: Acute healing of erosive esophagitis, active duodenal ulcers, and H. Pylori eradication. Excipients Light Magnesium Oxide / Mannitol / Methacrylic Acid Copolymer / Triethyl Citrate / Titanium Dioxide Alkaline Core Stabilizer / Diluent / Enteric Coating Polymer / Plasticizer (Engineered to absolutely block stomach acid and dissolve only in the alkaline duodenum) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 14-to-28 day acute gastroenterology dispensing regimens).
Racecadotril Capsules
FreeRacecadotril capsules are non-antibiotic, anti-diarrheal medications used primarily for the treatment of acute diarrhea. They are most commonly available in a 100 mg strength for adults.
Racecadotril Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet or Hard Gelatin Capsule, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density Alu-PVC blister strips to ensure the absolute chemical stability of the prodrug formulation.
Active Ingredient Strength Primary Clinical Function Racecadotril INN/Ph.Eur. 100 mg Global Clinical Standard: Adult dose for the rapid, anti-secretory resolution of acute diarrhea. Excipients Microcrystalline Cellulose / Pregelatinized Starch / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant (Engineered for immediate gastric dissolution and rapid conversion to the active metabolite, Thiorphan) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-7 day acute gastrointestinal dispensing regimens).
Ramipril & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet or Capsule, 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 Ramipril Ph.Eur./USP 5 mg (or 2.5 mg / 10 mg) ACE inhibition for vasodilation, RAAS blockade, and critical potassium retention. Hydrochlorothiazide Ph.Eur./USP 12.5 mg / 25 mg Global Clinical Standard: Thiazide diuretic for sodium excretion and sustained blood volume reduction. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Bicarbonate / Hypromellose / Magnesium Stearate Diluent / Superdisintegrant / Alkaline Stabilizing Agent (Engineered specifically to protect Ramipril from acidic degradation and moisture-induced cyclization) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict, high-compliance 30-day chronic cardiology dispensing regimens).
Ramipril and Amlodipine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Capsule or Film-Coated 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 Ramipril Ph.Eur./USP 5 mg / 10 mg ACE inhibition for vasodilation, neurohormonal blockade, and venous pressure equalization. Amlodipine (as Besilate) Ph.Eur./USP 5 mg / 10 mg Global Clinical Standard: Sustained CCB for profound, 24-hour arterial vasodilation. Excipients Microcrystalline Cellulose / Crospovidone / Sodium Stearyl Fumarate / Hypromellose / Iron Oxide Red Diluent / Superdisintegrant / Alkaline Stabilizing Lubricant (Engineered to protect Ramipril from acidic degradation and moisture) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict, high-compliance 30-day chronic cardiology dispensing regimens).
Ranitidine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Aqueous Solution in glass ampoules.
Active Ingredient Concentration Total Content & Format Ranitidine Hydrochloride USP/BP 25 mg / ml 50 mg in 2 ml Glass Ampoule Excipients Phenol / Potassium Di-hydrogen Phosphate Preservative / pH Buffer System (pH 6.7 to 7.3) *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Ranitidine Tablets
FreeRanitidine Hydrochloride Tablets IP
Each Filmcoated tablet contains :
Ranitidine Hydrochloride IP
Eq. To Ranitidine 150 mgRanitidine Hydrochloride Tablets IP
Each Filmcoated tablet contains :
Ranitidine Hydrochloride IP
Eq. To Ranitidine 300 mgRanitidine Hydrochloride Tablets USP
Each Filmcoated tablet contains :
Ranitidine Hydrochloride USP
Eq. To Ranitidine 300 mgUsage: – Indigestion, heartburn and acid reflux, gastro-esophageal reflux disease
Category: – Antacid & Anti ulcer drugs
Therapeutic category: – Antiulcer, Antacid
Ranolazine 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 bottles to ensure the absolute stability of the modified-release polymers.
Active Ingredient Strength Primary Clinical Function Ranolazine INN/Ph.Eur. 500 mg (Extended-Release) Global Clinical Standard: Base initiation dose for chronic angina management (taken twice daily). Ranolazine INN/Ph.Eur. 1000 mg (Extended-Release) Advanced maintenance dose for severe, refractory angina requiring maximum cellular relaxation. Excipients Hypromellose (HPMC) / Methacrylic Acid Copolymer / Microcrystalline Cellulose / Magnesium Stearate Hydrophilic Polymer Matrix / Enteric Matrix / Diluent (Engineered to form a viscous gel layer that controls the strict 12-hour drug diffusion rate) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 60 (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Rasagiline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated or Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly sensitive mesylate salt.
Active Ingredient Strength Primary Clinical Function Rasagiline Mesylate INN/Ph.Eur. 0.5 mg (Base Equivalent) Adjunct Standard: Initiating dose when used in combination with Levodopa. Rasagiline Mesylate INN/Ph.Eur. 1 mg (Base Equivalent) Global Clinical Standard: Maximum daily dose for monotherapy or advanced adjunct therapy. Excipients Mannitol / Maize Starch / Pregelatinized Starch / Colloidal Silicon Dioxide / Stearic Acid Diluent / Binder / Superdisintegrant / Glidant (Engineered for immediate gastric dissolution and rapid crossing of the blood-brain barrier) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict high-compliance 30-day chronic neurology dispensing regimens).
Rebamipide 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 the active mucosal agent.
Active Ingredient Strength Primary Clinical Function Rebamipide INN/Ph.Eur. 100 mg Global Clinical Standard: Mucosal protective agent for active ulcer healing and gastritis management. Excipients Microcrystalline Cellulose / Hydroxypropyl Methylcellulose (HPMC) / Croscarmellose Sodium / Magnesium Stearate Diluent / Premium Film-Coating / Superdisintegrant (Engineered for optimal gastric dispersion directly onto the mucosal lining) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic gastroenterology dispensing regimens).
Repaglinide & Metformin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or heavy-density PVC/PVDC blister strips to ensure the absolute chemical stability of the combined formulation.
Active Ingredient Strength Primary Clinical Function Repaglinide USP/Ph.Eur. 1 mg / 2 mg Short-acting meglitinide for rapid post-prandial (after-meal) insulin stimulation. Metformin Hydrochloride USP/Ph.Eur. 500 mg Global Clinical Standard: Biguanide for hepatic glucose suppression and insulin sensitization. Excipients Microcrystalline Cellulose / Povidone K30 / Croscarmellose Sodium / Poloxamer / Magnesium Stearate Diluent / Binder / Superdisintegrant / Surfactant (Engineered for immediate gastric dissolution and synchronized dual-absorption) *Pack Sizes: 10×10 or 3×10 Blisters (Optimized specifically for high-compliance 30-day chronic metabolic dispensing regimens tied directly to meal times).
Repaglinide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or heavy-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly sensitive meglitinide API.
Active Ingredient Strength Primary Clinical Function Repaglinide USP/Ph.Eur. 0.5 mg Base titration unit for treatment-naive patients or those with severe renal/hepatic impairment. Repaglinide USP/Ph.Eur. 1 mg / 2 mg Global Clinical Standard: Advanced maintenance doses for rapid post-prandial insulin stimulation. Excipients Microcrystalline Cellulose / Calcium Hydrogen Phosphate / Meglumine / Poloxamer / Magnesium Stearate Diluent / Stabilizer / Surfactant / Lubricant (Engineered for immediate gastric dissolution and ultra-fast systemic absorption) *Pack Sizes: 10×10 or 3×10 Blisters (Optimized specifically for high-compliance 30-day chronic metabolic dispensing regimens tied directly to meal times).
Ribavirin Capsules
FreeRibavirin capsules are antiviral medications typically used in combination with other drugs (like interferon or sofosbuvir) to treat chronic Hepatitis C. They are most commonly available in a 200 mg strength, though 100 mg versions also exist.
Ribavirin 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 heavy-density PVC/PVDC blister strips to ensure the stability of the active nucleoside analog and protect handlers from exposure.
Active Ingredient Strength Primary Clinical Function Ribavirin USP/Ph.Eur. 200 mg Global Clinical Standard: Base titration unit for precise, weight-based antiviral dosing. Ribavirin USP/Ph.Eur. 400 mg High-dose unit to drastically improve pill-burden compliance in heavy patients. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone / Magnesium Stearate Diluent / Superdisintegrant / Binder (Engineered for immediate gastric dissolution and rapid systemic absorption) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-dose, weight-based daily regimens requiring 4 to 6 tablets per day).
Rifampicin & Isoniazid Tablets
FreeProduct Composition & Strength (RH 300/150)
We supply this product in standardized Fixed-Dose Combinations (FDCs) as per international pharmacopoeial standards.
Active Ingredient Strength (per Tablet) Primary Clinical Function Rifampicin IP/BP/USP 300 mg The RNA Blocker: Sterilizing agent against TB bacilli. Isoniazid IP/BP/USP 150 mg The Wall Breaker: Potent bactericidal agent. Excipients Pharma Grade The Matrix: Ensures stability of the FDC. Rifampicin, Isoniazid & Pyrazinamide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Red/Brown). Stability is paramount as Rifampicin can degrade in the presence of Isoniazid if not properly formulated.
Active Ingredient Strength (Standard Adult) Strength (Pediatric) Therapeutic Role Rifampicin IP/BP/USP 150 mg 75 mg / 60 mg Broad Spectrum Sterilizer Isoniazid IP/BP/USP 75 mg 50 mg / 30 mg Cell Wall Inhibitor Pyrazinamide IP/BP/USP 400 mg 150 mg Intracellular Sterilizer Excipients Q.S. Ascorbic Acid (Stabilizer) Bioavailability Enhancer Rifampicin, Isoniazid & Pyrazinamide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Red/Brown). Stability is paramount as Rifampicin can degrade in the presence of Isoniazid if not properly formulated.
Active Ingredient Strength (Standard Adult) Strength (Pediatric) Therapeutic Role Rifampicin IP/BP/USP 150 mg 75 mg / 60 mg Broad Spectrum Sterilizer Isoniazid IP/BP/USP 75 mg 50 mg / 30 mg Cell Wall Inhibitor Pyrazinamide IP/BP/USP 400 mg 150 mg Intracellular Sterilizer Excipients Q.S. Ascorbic Acid (Stabilizer) Bioavailability Enhancer Risperidone Tablets
FreeRisperidone Tablets 1 mg
Each film coated tablet contains:
Risperidone IP 1 mgRisperidone Tablets 2 mg
Each film coated tablet contains:
Risperidone IP 2 mgRisperidone Tablets 3 mg
Each film coated tablet contains:
Risperidone IP 3 mgRisperidone Tablets 4 mg
Each film coated tablet contains:
Risperidone IP 4 mgRisperidone Tablets 1 mg
Each film coated tablet contains:
Risperidone BP 1 mgRisperidone Tablets 2 mg
Each film coated tablet contains:
Risperidone BP 2 mgRisperidone Tablets 3 mg
Each film coated tablet contains:
Risperidone BP 3 mgRisperidone Tablets 4 mg
Each film coated tablet contains:
Risperidone BP 4 mgUsage: – treat certain mental/mood disorders
Category: – Anti Anxiety drugs
Therapeutic category: – Antipsychotic, Antidepressant, CNS Drugs, Anti Anxiety
Risperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Orally Disintegrating Tablet (ODT) / Mouth Dissolving Tablet (MDT), packed exclusively in highly secure, moisture-resistant Alu-Alu or specialized Peelable Blister strips to protect the incredibly fragile, highly porous tablet structure.
Active Ingredient Strength Primary Clinical Function Risperidone INN/Ph.Eur. 1 mg / 2 mg Base titration units for acute agitation and pediatric/geriatric initiation. Risperidone INN/Ph.Eur. 4 mg Global Clinical Standard: High-dose therapy for severe, acute schizophrenic or manic exacerbations. Excipients Mannitol / Crospovidone / Aspartame / Peppermint Flavor / Magnesium Stearate Lyophilized Matrix Base / Superdisintegrant / Sweetener (Engineered to mask the bitter API and melt within seconds on the tongue) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict psychiatric ward dispensing and outpatient compliance regimens).
Rivaroxaban 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 potent DOAC molecule.
Active Ingredient Strength Primary Clinical Function Rivaroxaban INN/Ph.Eur. 2.5 mg Vascular Dose: Co-administered with Aspirin to prevent major cardiovascular events in CAD/PAD. Rivaroxaban INN/Ph.Eur. 10 mg Surgical Prophylaxis: Prevention of DVT following knee or hip replacement surgery. Rivaroxaban INN/Ph.Eur. 15 mg / 20 mg Global Clinical Standard: Treatment of acute DVT/PE and stroke prevention in Atrial Fibrillation. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Hypromellose / Sodium Lauryl Sulfate / Magnesium Stearate Diluent / Superdisintegrant / Surfactant (Engineered for optimal solubilization and synchronized gastrointestinal absorption) *Pack Sizes: 10×10 Alu-Alu Blisters or 14/28/30-Tablet Blisters (Optimized specifically for strict chronic cardiology and acute post-op dispensing regimens).
Rocuronium Bromide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Aqueous Solution in glass vials.
Active Ingredient Concentration Total Content & Format Rocuronium Bromide USP/BP 10 mg / ml 50 mg in 5 ml Glass Vial Rocuronium Bromide USP/BP 10 mg / ml 100 mg in 10 ml Glass Vial (High Volume) Excipients Sodium Acetate / Glacial Acetic Acid pH Buffer System (pH ~ 4.0) *Pack Sizes: Tray of 10 Vials.
Ropinirole Extended-Release
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 bottles to ensure the absolute stability of the modified-release polymers.
Active Ingredient Strength Primary Clinical Function Ropinirole HCl USP/Ph.Eur. 2 mg / 4 mg Base titration units for the slow, safe initiation of dopaminergic therapy. Ropinirole HCl USP/Ph.Eur. 8 mg Global Clinical Standard: Advanced maintenance dose for 24-hour continuous symptom control. (Higher total daily doses may be required). Excipients Hypromellose (HPMC) / Carmellose Sodium / Lactose Monohydrate / Magnesium Stearate Hydrophilic Polymer Matrix / Diluent / Lubricant (Engineered to form a viscous gel layer that controls the strict 24-hour drug diffusion rate) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 28/30 (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Rosuvastatin & Clopidogrel Capsules
FreeRosuvastatin and clopidogrel capsules are fixed-dose combination (FDC) medications used for the secondary prevention of cardiovascular events like heart attacks and strokes. They are typically available in strengths such as 10 mg/75 mg or 20 mg/75 mg.
Rosuvastatin & Fenofibrate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Bilayer or Matrix Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly sensitive Rosuvastatin calcium salt.
Active Ingredient Strength Primary Clinical Function Rosuvastatin Calcium INN/Ph.Eur. 10 mg or 20 mg (Equivalent to Rosuvastatin base) Potent HMG-CoA Reductase inhibition for massive LDL reduction and plaque stabilization. Fenofibrate (Micronized) INN/Ph.Eur. 160 mg (or 145 mg Nanoparticle) Global Clinical Standard: PPAR-alpha agonism for severe hypertriglyceridemia and HDL elevation. Excipients Lactose Monohydrate / Sodium Lauryl Sulfate / Crospovidone / Magnesium Stearate Diluent / Surfactant / Superdisintegrant (Engineered with heavy surfactant loading to force the insoluble Fenofibrate into systemic circulation) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for high-compliance 30-day chronic cardiology dispensing regimens).
Rosuvastatin Clopidogrel and Aspirin Capsules
FreeRosuvastatin, clopidogrel, and aspirin capsules are fixed-dose combination (FDC) medications used for the prevention of serious cardiovascular events such as heart attacks and strokes. This “triple therapy” combines a cholesterol-lowering statin with two antiplatelet agents
Rosuvastatin Tablets
FreeRucol
Rosuvastatin Tablets 10 mg
Each Film Coated Tablet Contains:
Rosuvastatin Calcium
eq. To Rosuvastatin 10 mgUsage: – treat certain mental/mood disorders
Category: – Anti Cardiovascular drugs
Therapeutic category: – Antilipidemic, Cardiovascular Agent
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
Sacubitril & Valsartan 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 chemical stability of the sensitive dual-molecule complex.
Active Ingredient Strength (Total Dose) Primary Clinical Function Sacubitril / Valsartan INN/Ph.Eur. 24 mg / 26 mg (50 mg Total) Starting dose for patients with severe renal impairment, hepatic impairment, or those not currently taking an ACEi/ARB. Sacubitril / Valsartan INN/Ph.Eur. 49 mg / 51 mg (100 mg Total) Standard Initiation Dose: For patients switching from standard doses of ACE inhibitors or ARBs. Sacubitril / Valsartan INN/Ph.Eur. 97 mg / 103 mg (200 mg Total) Target Maintenance Dose: Maximum adult therapy for optimal mortality reduction in heart failure. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Glidant (Engineered for immediate gastric dissolution and synchronized dual-absorption) *Pack Sizes: 14×2 or 28-Tablet Alu-Alu Blisters (Optimized specifically for strict twice-daily chronic cardiology dispensing regimens).
Salbutamol & Theophylline 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 both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Salbutamol Sulphate BP/Ph.Eur. 2 mg (Equivalent to Salbutamol base) Rapid-onset beta-2 agonism for immediate smooth muscle relaxation. Theophylline (Anhydrous) BP/Ph.Eur. 100 mg Global Clinical Standard: PDE inhibition for sustained bronchodilation and mild respiratory anti-inflammation. Excipients Microcrystalline Cellulose / Maize Starch / Purified Talc / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered for strict, synchronized gastric dissolution) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-compliance 30-day chronic pulmonology dispensing regimens).
Salbutamol Inhaler
FreeSalbutamol Inhaler Metered-Dose Inhaler
Product Composition & Strength
We supply this product in standardized Metered-Dose Inhaler (MDI) formats, optimized for direct pulmonary delivery.
Component Strength (per actuation) Primary Clinical Function Salbutamol (as Sulfate) IP/BP 100 mcg The Rescue Agent: Instantly opens airways. Propellant HFA-134a (CFC-Free) The Carrier: Ensures ozone-friendly delivery. Formulation Pressurized Aerosol The Standard: 200 metered doses per canister. Salbutamol Tablets
FreeSalbutamol Tablets IP 2 mg Each Uncoated Tablet contains: Salbutamol Sulphate IP – Equivalent to Salbutamol 2 mg
Excipients – QSSalbutamol Tablets IP 4 mg Each uncoated tablets contains: Salbutamol Sulphate IP –
Equivalent to Salbutamol 4 mg
Excipients – QSSalbutamol Tablets BP
Each Uncoated tablet contains:
Salbutamol Sulphate BP
Eq. to Salbutamol 4 mgUsage: – treat wheezing and shortness of breath caused by breathing problems
Category: – Antacid & Anti ulcer drugs
Therapeutic category: – Antiasthmatic
Saxagliptin 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 sensitive active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Saxagliptin (as Hydrochloride) INN/Ph.Eur. 2.5 mg Target dose for patients with moderate/severe renal impairment or those taking strong CYP3A4 inhibitors. Saxagliptin (as Hydrochloride) INN/Ph.Eur. 5 mg Global Clinical Standard: Maximum adult daily dose for the maintenance of Type 2 Diabetes. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate Diluent / Binder / Superdisintegrant (Engineered for immediate gastric dissolution and optimal bioavailability) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for high-compliance 30-day chronic metabolic dispensing regimens).
Secnidazole Tablets
FreeSecnidazole Tablets IP 500 mg
Each Filmcoated tablet contains :
Secnidazole IP 500 mgSecnidazole Tablets I.P.
Each Filmcoated tablet contains :
Secnidazole IP 1 gmSeczole -2 Secnidazole Tablets IP 2 gm
Each film coated tablet contains:
Secnidazole IP 2 gmUsage: – treat vaginal infection (vaginosis) caused by bacteria
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
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
Secnidazole Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Off-White). The high-dose tablet is designed for ease of swallowing.
Active Ingredient Strength (Standard) Therapeutic Role Secnidazole USP/BP 500 mg Pediatric / Divided Dose Secnidazole USP/BP 1000 mg (1g) Standard Adult Dose (2 tablets = 2g) Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Binder / Disintegrant Serratiopeptidase Tablets
FreeSERRATIOPTIDASE TABLETS 5 MG
Enteric Coated Tablet:
Serratiopeptidase 10000 Serratiopeptidase unit 5 MG
Usage: – back pain, osteoarthritis, rheumatoid arthritis, osteoporosis, fibromyalgia, carpel tunnel syndrome, migraine headache, and tension headache
Category: – Anti-inflammatory drug (NSAIDs)
Therapeutic category: – Anti-inflammatory
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Sertaconazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed Vaginal Tablet (Pessary), packed exclusively in highly secure, moisture-resistant Alu-PVC blister strips. Each tablet is often packaged with a hygienic, medical-grade disposable applicator to ensure proper and comfortable insertion.
Active Ingredient Strength Primary Clinical Function Sertaconazole Nitrate BP/Ph.Eur. 500 mg Global Clinical Standard: Single-dose acute therapy for the complete eradication of vaginal Candida infections. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Adipic Acid / Sodium Bicarbonate / Magnesium Stearate Diluent / Effervescent Base (Engineered to rapidly dissolve in the low-moisture vaginal environment and disperse evenly across the mucosal walls) *Pack Sizes: 1 Tablet per Blister Box + 1 Disposable Applicator (Optimized specifically for premium, high-turnover OTC pharmacy shelves and acute gynecology dispensing).
Sertraline Tablets
FreeSertraline Tablet IP 50 mg
Each Filmcoated Tablet Contains:
Sertraline Hydrochloride
eq. To Sertraline 50 mgUsage: – Treat depression
Category: – Anti Anxiety drugs
Therapeutic category: – Antipsychotic, Antidepressant, CNS Drugs, Anti Anxiety
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
Sevelamer Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles to prevent the highly hygroscopic polymer from absorbing ambient humidity and expanding.
Active Ingredient Strength Primary Clinical Function Sevelamer Carbonate INN/Ph.Eur. 800 mg Global Standard: High-dose adult therapy for the aggressive management of hyperphosphatemia. Sevelamer Carbonate INN/Ph.Eur. 400 mg Base titration unit for specific dietary adjustments and milder phosphate elevations. Excipients Microcrystalline Cellulose / Hypromellose / Diacetylated Monoglycerides / Colloidal Silicon Dioxide / Zinc Stearate Diluent / Premium Film-Coating / Glidant / Lubricant (Engineered for structural integrity and smooth swallowing) *Pack Sizes: Bottles of 30, 90, or 270 Tablets (Optimized specifically for strict, massive-volume daily dialysis regimens where patients consume multiple grams with every meal).
Sildenafil Citrate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically Blue, Diamond-Shaped). The coating is essential to mask the extremely bitter taste of the citrate salt.
Active Ingredient Strength (Standard) Therapeutic Role Sildenafil Citrate USP/BP 25 mg Initiation / Renal Impairment Sildenafil Citrate USP/BP 50 mg Standard Adult Dose Sildenafil Citrate USP/BP 100 mg Maximum Efficacy Dose Excipients Q.S. Microcrystalline Cellulose / Indigo Carmine Binder / Blue Colorant Sildenafil Citrate oral jelly
FreeProduct Composition & Strength
We supply this product as a Single-Dose Liquid Jelly Sachet, optimized for portability and discreet use.
Active Ingredient Strength (per 5g sachet) Primary Clinical Function Sildenafil Citrate IP/BP 100 mg The PDE5 Inhibitor: Restores erectile function. Excipients Glycerin / Sodium CMC The Vehicle: Ensures smooth jelly texture and stability. Flavoring Orange / Strawberry / Pineapple / Butterscotch The Palatable Base: Improves patient compliance. Silodosin 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 active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Silodosin INN/Ph.Eur. 8 mg Global Clinical Standard: Maximum adult daily dose for the rapid relief of lower urinary tract symptoms (LUTS) associated with BPH. Excipients Mannitol / Pregelatinized Starch / Sodium Stearyl Fumarate / Hypromellose / Titanium Dioxide Diluent / Binder / Lubricant / Film-Coating (Engineered for highly synchronized gastric dissolution and optimal bioavailability) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for high-compliance 30-day urology dispensing regimens).
Sirolimus Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Nano-crystal Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute kinetic stability of the sensitive macrolide API.
Active Ingredient Strength Primary Clinical Function Sirolimus USP/Ph.Eur. 1 mg Global Standard: Base titration unit for precise blood-level adjustments in renal transplant recipients. Sirolimus USP/Ph.Eur. 2 mg Standard daily maintenance dose (following initial loading protocols). Excipients Macrogol / Microcrystalline Cellulose / Sucrose / Povidone / Magnesium Stearate Solid Dispersion Carrier / Diluent / Binder (Engineered to drastically enhance the systemic absorption of the highly insoluble API) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 100 (Optimized specifically for strict, life-long transplant adherence regimens).
