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Abacavir & Lamivudine Tablets.
FreeProduct Composition & Strength
We supply this product in the globally standardized “600/300” ratio, optimized for maximum efficacy with a convenient once-daily dosing schedule.
Active Ingredient Strength Primary Clinical Function Abacavir (as Sulfate) USP/BP 600 mg The Guanosine Analogue: Stops viral DNA synthesis by mimicking the guanosine building block. Lamivudine USP/BP 300 mg The Cytidine Analogue: A highly potent NRTI that works synergistically to block the reverse transcriptase enzyme. Excipients Proprietary Matrix Bio-Stable Coating: Engineered to ensure consistent absorption and protect the APIs from environmental degradation. Abacavir Tablets
FreeProduct Composition & Strength
We supply this product in standardized strengths to allow for both adult and pediatric weight-based dosing.
Active Ingredient Strength Primary Clinical Function Abacavir (as Sulfate) USP/BP/Ph.Eur. 300 mg The Standard Dose: Usually taken twice daily as part of a multi-drug regimen. Abacavir (as Sulfate) USP/BP/Ph.Eur. 600 mg The Once-Daily Anchor: Optimized for patient compliance in simplified treatment schedules. Excipients Proprietary Matrix Bio-Stable System: Engineered to ensure consistent oral absorption and protect the API from environmental degradation. Abiraterone acetate Tablets
FreeProduct Composition & Strength
We supply this product in standardized strengths designed for high-dose oncology regimens.
Active Ingredient Strength Primary Clinical Function Abiraterone Acetate USP/Ph.Eur. 250 mg The Standard Unit: Used in a 4-tablet daily regimen to reach the 1000 mg therapeutic dose. Abiraterone Acetate USP/Ph.Eur. 500 mg The High-Compliance Unit: Reduces “pill burden” for elderly patients (2 tablets daily). Excipients Micronized Matrix Enhanced Bioavailability: Engineered to ensure consistent absorption of this lipophilic (fat-soluble) molecule. 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 Acebrophylline (SR) Montelukast & Fexofenadine Tablets
FreeProduct Composition & Strength
We supply this product as a Sustained-Release, Film-Coated Tablet, engineered to provide a steady-state therapeutic concentration over a full 24-hour cycle.
Active Ingredient Strength Primary Clinical Function Acebrophylline (SR) USP/BP 200 mg The Broncho-Mucolytic: Relaxes airways and thins mucus for 24-hour breathing comfort. Montelukast (as Sodium) USP/BP 10 mg The LTRA: Prevents chronic inflammation and asthma triggers in the lungs. Fexofenadine HCl USP/BP 120 mg The Antihistamine: Provides non-sedating relief from upper respiratory allergic symptoms. Acebrophylline & Montelukast Tablets
FreeProduct Composition & Strength
We supply this product as a Sustained-Release, Film-Coated Tablet, engineered to provide synchronized therapeutic levels with convenient once-daily dosing.
Active Ingredient Strength Primary Clinical Function Acebrophylline (SR) USP/BP 200 mg The Airway Opener: Provides 24-hour bronchodilation and thins thick mucus. Montelukast (as Sodium) USP/BP 10 mg The Inflammation Blocker: Prevents asthma triggers and reduces lung swelling. Excipients Hydrophilic Matrix Controlled-Release System: Engineered to provide a smooth plasma curve, minimizing heart palpitations. Acebrophylline Tablets
FreeProduct Composition & Strength
We supply this product as both an Immediate-Release Tablet for acute management and a Sustained-Release (SR) Tablet for 24-hour protection.
Active Ingredient Strength Primary Clinical Function Acebrophylline USP/BP 100 mg The Standard Relief Unit: Taken twice daily to manage active symptoms of bronchitis and asthma. Acebrophylline USP/BP 200 mg SR The 24-Hour Anchor: A sustained-release format that provides consistent airway stability with once-daily dosing. Excipients Hydrophilic Matrix Controlled-Release System: Engineered to provide a smooth plasma concentration curve, minimizing the risk of “Theophylline-like” side effects. 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 & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as a Film-Coated Tablet, engineered for rapid disintegration and synchronized absorption.
Active Ingredient Strength Primary Clinical Function Aceclofenac USP/BP 100 mg The Anti-Inflammatory: Targets tissue inflammation and reduces joint stiffness. Paracetamol USP/BP 325 mg / 500 mg The Analgesic: Provides rapid relief from acute pain and manages fever. Excipients Proprietary Matrix Rapid-Release System: Engineered to ensure both APIs reach therapeutic levels within 30–60 minutes. Aceclofenac & Thiocolchicoside Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the semi-synthetic Thiocolchicoside component.
Active Ingredient Strength Primary Clinical Use Aceclofenac BP/Ph.Eur.
Thiocolchicoside INN/Ph.Eur.100 mg
4 mgStandard Orthopedic Dose: Twice-daily therapy for moderate-to-severe acute back pain and torticollis. Aceclofenac BP/Ph.Eur.
Thiocolchicoside INN/Ph.Eur.100 mg
8 mgSevere Trauma Dose: Maximum therapy for severe, immobilizing orthopedic spasms (strictly twice daily). Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate Diluent / Superdisintegrant (Engineered for immediate gastric dissolution and rapid onset of relief) Aceclofenac Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. We utilize advanced solubilizing agents to ensure the drug remains stable in liquid form.
Active Ingredient Strength (Standard) Therapeutic Role Aceclofenac BP/IP 150 mg / ml Analgesic / Anti-inflammatory Excipients Q.S. Benzyl Alcohol / Propylene Glycol Preservative / Co-solvent *Pack Sizes: Tray of 5 Ampoules (1ml each) or 10 Ampoules.
Aceclofenac Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Standard) or Sustained Release (SR) Tablets.
Active Ingredient Strength Release Type Role Aceclofenac IP/BP/USP 100 mg Immediate Release Standard Adult Dose Aceclofenac IP/BP/USP 200 mg Sustained Release (SR) Once Daily Dosing Excipients Q.S. — Disintegrant / Binder 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. Acenocoumarol Tablets
FreeProduct Composition & Strength
We supply this product in multiple strengths to allow for the precise, micro-gram level titration required for safe anticoagulation.
Active Ingredient Strength Primary Clinical Function Acenocoumarol USP/BP/Ph.Eur. 1 mg / 2 mg The Titration Unit: Used for fine-tuning the maintenance dose to keep the INR within the target range (usually 2.0–3.0). Acenocoumarol USP/BP/Ph.Eur. 3 mg / 4 mg The Loading/Anchor Dose: Used for initial therapy or for patients requiring higher systemic anticoagulation. Excipients Proprietary Matrix Bio-Stable System: Engineered to ensure consistent oral absorption and predictable pharmacokinetics. Acetaminophen & Tramadol Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product in the globally standardized “325/37.5” ratio, optimized for maximum efficacy with minimal opioid-related side effects.
Active Ingredient Strength Primary Clinical Function Acetaminophen (Paracetamol) USP/BP 325 mg The Rapid Starter: Provides quick onset of analgesia and antipyretic (fever-reducing) effects. Tramadol Hydrochloride USP/BP 37.5 mg The Sustained Blocker: Provides moderate-to-severe pain relief via opioid and neurotransmitter pathways. Excipients Proprietary Matrix Bio-Synchronized System: Engineered to ensure both APIs reach therapeutic plasma levels simultaneously for a synergistic effect. Acetazolamide Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White, round). The 250 mg strength is the universal standard.
Active Ingredient Strength (Standard) Primary Role Acetazolamide USP/BP/IP 250 mg Glaucoma / Altitude Sickness / Edema Excipients Q.S. Starch / Povidone / Sodium Starch Glycolate Acetyl Salicylic Acid Tablets
FreeProduct Composition & Strength
We supply this product in two distinct clinical ranges: the “Cardio-Shield” range and the “Analgesic-Power” range.
Active Ingredient Strength Primary Clinical Function Acetylsalicylic Acid USP/BP 75 mg / 100 mg The Cardio-Shield: Once-daily “Baby Aspirin” for long-term prevention of heart attack and stroke. Acetylsalicylic Acid USP/BP 300 mg The Emergency Loading Dose: Used immediately during a suspected heart attack to break up clots. Acetylsalicylic Acid USP/BP 500 mg The Analgesic Anchor: For the relief of headache, toothache, and musculoskeletal pain. 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). Activated Charcoal Tablets
FreeProduct Composition & Strength
We supply this product as a High-Density, Compressible Tablet, engineered to disintegrate rapidly in the stomach for maximum surface area exposure.
Active Ingredient Strength Primary Clinical Function Activated Charcoal USP/BP/Ph.Eur. 250 mg The GI Relief Unit: Used primarily for over-the-counter (OTC) management of gas and bloating. Activated Charcoal USP/BP/Ph.Eur. 500 mg The Emergency Payload: High-potency format for clinical detoxification and poisoning management. Excipients Binder/Disintegrant Rapid-Discharge Matrix: Engineered to ensure the charcoal particles disperse immediately upon contact with gastric fluid. Acyclovir Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated, Dispersible Tablets (often flavored/sweetened for palatability), packed in moisture-resistant blister strips.
Active Ingredient Strength Primary Clinical Use Acyclovir USP/BP/Ph.Eur. 200 mg HSV-1 & HSV-2 (Genital/Labial Herpes) Treatment Acyclovir USP/BP/Ph.Eur. 400 mg Recurrent HSV Suppression / Chronic Prophylaxis Acyclovir USP/BP/Ph.Eur. 800 mg Varicella (Chickenpox) & Herpes Zoster (Shingles) Excipients Crospovidone / Aspartame / Flavoring Agents Superdisintegrant / Sweetener / Taste-Masking Acyclovir injection
Freecomposition
Aciclovir 400 mg
Each Uncoated contains:
Aciclovir IP 400 mg
Excipients – QSAciclovir 200 mg
Each Uncoated Contains :
Aciclovir 200 mg
Excipients q.sUsage :- Treat infections caused by certain types of viruses
Category :- Antibiotic drugs
Therapeutic category :- Antiviral
Pcd pharma franchise :-
Pcd marketing :-
Manufacturer :- Healthy Life Pharma Pvt Ltd
Exporter :- Healthy Inc
Supplier :- Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor :- Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller :- Healthy Life Pharma Pvt Ltd
Healthy Inc
Acyclovir Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Dispersible Tablets (DT). The dosage varies significantly based on the viral strain being treated.
Active Ingredient Strength (Standard) Primary Indication Acyclovir USP/BP/IP 200 mg Herpes Simplex (Genital/Labial) Acyclovir USP/BP/IP 400 mg Suppression / Prophylaxis Acyclovir USP/BP/IP 800 mg Shingles (Herpes Zoster) / Chickenpox Excipients Q.S. Disintegrant / Binder 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. Adrenaline Injections
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. The formulation includes stabilizers to prevent rapid oxidation.
Active Ingredient Strength (Standard 1:1000) Therapeutic Role Adrenaline Bitartrate BP/USP Eq. to Adrenaline 1 mg / ml Vasopressor / Bronchodilator Excipients Q.S. Sodium Metabisulfite / Sodium Chloride Antioxidant / Isotonicity *Pack Sizes: Tray of 10 Ampoules (1ml each) or Box of 50/100 Ampoules (Hospital Pack).
Adrenochrome Monosemicarbazone Tablet
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (often Orange/Red) to protect the drug from oxidation and light.
Active Ingredient Strength (Standard) Formulation Type Primary Role Adrenochrome Monosemicarbazone 10 mg Sugar Coated Tablet Minor Bleeding / Maintenance Adrenochrome Monosemicarbazone 25 mg / 30 mg Sugar Coated Tablet Surgical Prophylaxis Excipients Q.S. Titanium Dioxide / Sucrose Light Protection Coating 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. Agomelatine 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 API.
Active Ingredient Strength Primary Clinical Function Agomelatine USP/Ph.Eur. 25 mg The Therapeutic Anchor: The globally validated dose for restoring circadian rhythm and treating major depression. Excipients Proprietary Matrix Bio-Synchronized Release: Engineered to ensure a rapid $T_{max}$ (approx. 1-2 hours) to align with the body’s natural melatonin surge. Albendazole Tablet
Freeduct Composition & Strength
We supply this product as Chewable Tablets (Fruit Flavored) or Standard Film Coated Tablets. The chewable format is critical for Mass Drug Administration (MDA) in children.
Active Ingredient Strength (Standard) Formulation Type Role Albendazole USP/BP 200 mg Chewable / Film Coated Pediatric (1-2 Years) Albendazole USP/BP 400 mg Chewable (Uncoated) Standard Adult / MDA Dose Albendazole USP/BP 400 mg Film Coated Systemic Therapy Excipients Q.S. Mannitol / Orange Flavor Palatability Alendronate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Oval). The 70 mg strength is the international standard for weekly administration.
Active Ingredient Strength (Standard) Dosing Frequency Role Alendronate Sodium USP/BP 10 mg Once Daily Maintenance / Male Osteoporosis Alendronate Sodium USP/BP 70 mg Once Weekly Postmenopausal Osteoporosis Excipients Q.S. — Disintegrant / Filler Alfacalcidol Softgel Capsules
FreeProduct Composition & Strength
We supply this product as a Liquid-Filled Soft Gelatin Capsule, packed in highly protective, opaque blister strips to prevent the extreme light-degradation associated with vitamin D analogues.
Active Ingredient Strength Primary Clinical Use Alfacalcidol BP/EP 0.25 mcg (Micrograms) Initial Titration / Pediatric / Maintenance Dosing Alfacalcidol BP/EP 0.5 mcg (Micrograms) Standard Adult Dialysis / Osteoporosis Dosing Alfacalcidol BP/EP 1.0 mcg (Micrograms) Severe Hypocalcemia / High-PTH Suppression Excipients Refined Arachis (Peanut) Oil / BHA Lipid Carrier System / Antioxidant Stabilizer *Pack Sizes: 10×10 Opaque Alu-PVC Blisters or Alu-Alu Blisters. (Opaque packaging is an absolute necessity to maintain microgram API stability).
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. Allopurinol Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration).
Active Ingredient Strength (Standard) Role Allopurinol IP/BP/USP 100 mg Initial Dose / Renal Adjustment Allopurinol IP/BP/USP 300 mg Standard Maintenance Dose Excipients Q.S. Binder / Disintegrant Allylestrenol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bio-Stable Tablet, packed in high-barrier Alu-Alu blister strips to ensure hormonal stability.
Active Ingredient Strength Primary Clinical Function Allylestrenol USP/BP/Ph.Eur. 5 mg The Standard OB-GYN Anchor: The globally validated dose for maintaining the corpus luteum and supporting the early placenta. Excipients Proprietary Matrix Bio-Synchronized System: Engineered to ensure rapid oral absorption and high plasma concentration to provide immediate uterine stability. 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. Alpha Ketoanalogue Tablets
FreeProduct Composition & Strength
We supply this product as a Multi-Mineral, Amino Acid Complex, carefully balanced to meet the Nutritional Requirements of Uremic Patients.
Component (Active) Amount per Tablet Clinical Function Alpha-Keto-Isoleucine / Leucine / Valine / Phenylalanine Calcium Salts The Protein Builders: Converted into essential amino acids using waste nitrogen. Alpha-Hydroxy-Methionine Calcium Salt The Sulfur Source: Provides the essential hydroxy-analog of methionine. L-Lysine / L-Threonine / L-Tryptophan Acetate/Pure Form Essential Amino Acids: Direct supplementation of AA that the body cannot synthesize. L-Histidine / L-Tyrosine Pure Form Conditional Amino Acids: Critical for maintaining nitrogen balance in renal failure. Calcium Content ~50 mg (approx) Phosphate Binder Support: Provides calcium which helps in managing hyperphosphatemia. Alprazolam & Sertraline Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the benzodiazepine component.
Active Ingredient Strength Primary Clinical Function Sertraline (as HCl) USP/BP 25 mg / 50 mg The Antidepressant Anchor: Provides long-term correction of serotonin levels to treat depression and OCD. Alprazolam USP/BP 0.25 mg / 0.5 mg The Anxiolytic Bridge: Provides rapid relief from acute anxiety and prevents panic spikes. Excipients Proprietary Matrix Bio-Synchronized System: Engineered to ensure the rapid release of Alprazolam for immediate relief while Sertraline maintains steady-state plasma levels. 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.
Aluminium hydroxide Magnesium Trisilicate Tablet
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (Mint/Orange Flavor). The chewable format is essential to increase the surface area for rapid reaction.
Active Ingredient Strength (Standard) Role Dried Aluminium Hydroxide Gel USP/BP 250 mg Acid Neutralizer / Astringent Magnesium Trisilicate USP/BP 500 mg Acid Neutralizer / Adsorbent Excipients Q.S. Mannitol / Menthol (Flavor) 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. Amikacin Sulphate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid in Glass Vials or Ampoules. The solution is clear, colorless to pale yellow, and requires no reconstitution (ready-to-use).
ant Active Ingredient Strength (Standard) Therapeutic Role Amikacin Sulphate USP/BP 100 mg / 2 ml Pediatric Dose Amikacin Sulphate USP/BP 250 mg / 2 ml Intermediate Dose Amikacin Sulphate USP/BP 500 mg / 2 ml Adult Standard Dose Excipients Q.S. Sodium Citrate / Sodium Metabisulfite Buffer / Antioxid *Pack Sizes: Tray of 10 Ampoules or Box of 1/10 Vials.
Amiloride & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product in the globally standardized strength ratio, packed in high-barrier Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Amiloride (as HCl) USP/BP 5 mg The Potassium Guard: Prevents the loss of potassium, protecting against heart arrhythmias and muscle weakness. Hydrochlorothiazide USP/BP 50 mg The Volume Reducer: Excretes excess sodium and water to reduce the load on the heart and vessels. Excipients Proprietary Matrix Steady-State Release System: Engineered to ensure a consistent diuretic effect over a full 24-hour cycle. Aminosalicylic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Delayed-Release (DR) Tablet, packed in moisture-resistant Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function 4-Aminosalicylic Acid USP/BP 500 mg The Standard Titration Unit: Allows for gradual dose escalation to manage gastrointestinal side effects. 4-Aminosalicylic Acid USP/BP 1000 mg The Maintenance Payload: High-dose format for adult MDR-TB regimens requiring up to 8–12g daily. Excipients Acid-Resistant Polymer Enteric Shield System: Engineered to bypass the stomach and release the API in the upper intestine for maximum absorption. 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 injection
FreeComposition
Amiodarone 150 mg / 3 ml ( leaflet inside ) ( 24 months shelf life )
Pcd pharma franchise:-
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
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. Amisulpride Tablets
FreeProduct Composition & Strength
We supply this product in a full range of strengths to facilitate both low-dose “Disthymia” protocols and high-dose “Schizophrenia” maintenance.
Active Ingredient Strength Primary Clinical Function Amisulpride USP/BP 50 mg / 100 mg The Negative Symptom Unit: Used to treat social withdrawal, depression, and lack of initiative. Amisulpride USP/BP 200 mg The Transition Anchor: Used for moderate psychosis or as a step-up dose during titration. Amisulpride USP/BP 400 mg The Positive Symptom Payload: High-potency dose for acute psychotic episodes and hallucinations. Amitriptyline & Chlordiazepoxide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the benzodiazepine component.
Active Ingredient Strength Primary Clinical Function Amitriptyline (as HCl) USP/BP 12.5 mg / 25 mg The Antidepressant Anchor: Elevates mood and energy levels by modulating neurotransmitter reuptake. Chlordiazepoxide USP/BP 5 mg / 10 mg The Anxiolytic Shield: Provides rapid relief from nervousness, agitation, and muscle tension. Excipients Proprietary Matrix Bio-Synchronized System: Engineered to ensure the rapid onset of the anxiolytic effect while the antidepressant effect builds over time. Amitriptyline Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often Blue, Yellow, or Orange depending on strength) to mask the intensely bitter taste of the API.
Active Ingredient Strength (Standard) Primary Role Amitriptyline HCl IP/BP/USP 10 mg Neuropathic Pain / Migraine / Sleep Amitriptyline HCl IP/BP/USP 25 mg Pain / Depression Initiation Amitriptyline HCl IP/BP/USP 50 mg Major Depression (Maintenance) Amitriptyline HCl IP/BP/USP 75 mg High Potency / Severe Depression Amlodipine & 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 & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, engineered for synchronized 24-hour hemodynamic control.
Active Ingredient Strength Primary Clinical Function Amlodipine (as Besylate) USP/BP 5 mg / 10 mg The Vasodilator: Reduces the resistance of blood vessels to lower systemic pressure. Hydrochlorothiazide USP/BP 12.5 mg / 25 mg The Volume Reducer: Excretes excess sodium and water to reduce circulatory load. Excipients Proprietary Matrix Steady-State System: Engineered to ensure consistent plasma concentrations of both drugs to prevent “dips” in BP control. 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 Tablet
FreeAmlodipine Tablets IP 5 mg
Each Uncoated tablet contains :
Amlodipine Besylate IP
Eq to Amlodipine 5 mgAmlodipine Tablets IP 10 mg
Each Uncoated Tablet Contains :
Amlodipine Besylate IP
Eq To Amlodipine 10 mgAmlodipine Besylate Tablets IP 2.5 mg
Each uncoated tablet contains :
Amlodipine Besylate IP
Eq. To Amlodipine 2.5 mgAmlodipine Besylate Tablets IP 2.5 mg
Each Film Coated Tablet Contains:
Amlodipine Besylate IP
eq. To Amlodipine 2.5 mgAmlodipine Besylate Tablets IP 5 mg
Each Film Coated Tablet Contains:
Amlodipine Besylate IP
eq. To Amlodipine 5 mgAMLODIPINE & ENALAPRIL MALEATE TABLET
Each Film Coated Tablet Contains :
Amlodipine Besylate
Eq. To Amlodipine 5 mg
Enalapril Maleate 5 mg
Excipients q.sAMLODIPINE & LISINOPRIL TABLET
Each Film Coated Tablet Contains :
Amlodipine Besylate
Eq. To Amlodipine 5 mg
Lisinopril dihydrate
Eq. To Lisinopril 5 mg
Excipients q.sTRIPPLEACE AMLODIPINE -10 / AMLODIPINE
TABLETS 10 MG
Each uncoated tablet contains:
Amlodipine Besilate BP
Equivalent to Amlodipine 10 mg
Excipients Q.S.Usage: – Treat high blood pressure
Category: – Hypertensive / Cardiac Drugs
Therapeutic category: – hypertensive, Cardiovascular Agent,
Amodiaquine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Yellow) or Film Coated Tablets. The strength is typically expressed in terms of the Amodiaquine Base.
Active Ingredient Strength (Base Equivalent) Salt Content (Approx) Role Amodiaquine HCl USP/BP 67.5 mg ~ 90 mg Pediatric (ACT Component) Amodiaquine HCl USP/BP 153 mg / 150 mg ~ 200 mg Adolescent / Co-blistered Amodiaquine HCl USP/BP 200 mg ~ 260 mg Standard Adult Dose Excipients Q.S. Microcrystalline Cellulose / Magnesium Stearate Direct Compression Amoxapine Tablets
FreeProduct Composition & Strength
We supply this product in a full range of strengths to allow for precise clinical titration, packed in high-barrier Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Amoxapine USP/BP 25 mg / 50 mg The Titration Unit: Used for gradual dose escalation to minimize initial sedative effects. Amoxapine USP/BP 100 mg The Standard Anchor: The primary maintenance dose for outpatients with moderate depression. Amoxapine USP/BP 150 mg The High-Potency Payload: For hospitalized patients with severe psychotic or endogenous depression. Amoxicillin & Potassium Clavulanate Dispersible Tablets
FreeProduct Composition & Strength
We supply this product in the globally standardized 7:1 ratio, packed in high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive Clavulanate.
Active Ingredient Strength Primary Clinical Function Amoxicillin (as Trihydrate) USP/BP 200 mg / 400 mg The Growth Inhibitor: Destroys the bacterial cell wall across a broad range of pathogens. Potassium Clavulanate USP/BP 28.5 mg / 57 mg The Resistance Shield: Neutralizes bacterial enzymes, allowing Amoxicillin to function. Excipients Sweetened Matrix Pediatric-Friendly System: Engineered with pleasant fruit flavors to ensure 100% child compliance. Amoxicillin & Potassium Clavulanate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, ultra-low moisture Alu-Alu blister strips (often containing integrated desiccants) to ensure the absolute stability of the incredibly hygroscopic Clavulanate salt.
Active Ingredient Strength Primary Clinical Function Amoxicillin Trihydrate USP/Ph.Eur.
Potassium Clavulanate USP/Ph.Eur.500 mg
125 mg
(Total: 625 mg)Standard Adult Dose: Therapy for moderate RTIs, dental infections, and skin infections. Amoxicillin Trihydrate USP/Ph.Eur.
Potassium Clavulanate USP/Ph.Eur.875 mg
125 mg
(Total: 1000 mg)High-Dose Adult Therapy: Aggressive intervention for severe pneumonia, severe sinus infections, and bite wounds. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Moisture Scavenger (Engineered for immediate gastric dissolution) *Pack Sizes: 1×6 or 1×10 Alu-Alu Blisters (Optimized specifically for strict 5-to-7 day acute antibiotic regimens).
Amoxicillin Capsules
FreeAmoxicillin capsules are common penicillin-type antibiotics typically available in 250 mg and 500 mg strengths.
Amoxicillin Sodium Injection 250mg
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Pediatric Dose) Therapeutic Role Amoxicillin Sodium USP/BP Equivalent to 250 mg Amoxicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Amoxicillin Sodium Injection 500mg
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard Adult Dose) Therapeutic Role Amoxicillin Sodium USP/BP Equivalent to 500 mg Amoxicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Amoxicillin Trihydrate Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Fruit-Flavored Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive API.
Active Ingredient Strength Primary Clinical Function Amoxicillin (as Trihydrate) USP/BP 125 mg The Pediatric Starter: Ideal for infants and toddlers requiring low-dose respiratory or ear infection therapy. Amoxicillin (as Trihydrate) USP/BP 250 mg The Junior Anchor: The standard dose for older children and adolescents for broad-spectrum anti-infective coverage. Excipients Sweetened Matrix Taste-Masking System: Engineered with pleasant flavors (Strawberry/Pineapple/Orange) to overcome the natural bitterness of the antibiotic. Amoxycillin , Cloxacillin And Lactic Acid Bacillus Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet or Capsule, packed in high-barrier Alu-Alu blister strips to ensure the stability of the live probiotic spores.
Active Ingredient Strength Primary Clinical Function Amoxycillin (as Trihydrate) USP/BP 250 mg The Growth Inhibitor: Destroys the bacterial cell wall across a broad range of pathogens. Cloxacillin (as Sodium) USP/BP 250 mg The Defense Breaker: Specifically neutralizes bacterial enzymes, making the treatment effective against “Staph” infections. Lactic Acid Bacillus (LAB) 1.5 Billion Spores The Biological Shield: Replenishes healthy gut bacteria to prevent diarrhea and boost immunity. Amoxycillin & Cloxacillin Capsules
FreeAmoxycillin and cloxacillin capsules (commonly known as co-amoxiclox) are combination antibiotics used to treat infections where bacteria might produce enzymes that resist standard penicillin. They are typically available in a 500 mg total strength (250 mg / 250 mg)
Amoxycillin & Dicloxacillin Capsules
FreeAmoxycillin and dicloxacillin capsules are combination antibiotics designed to broaden the spectrum of treatment while protecting the medicine from bacterial resistance. They are typically available in a 500 mg total strength (often 250 mg / 250 mg)
Amoxycillin & Potassium Clavulanate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The ratio is critically balanced (usually 5:1) for optimal pharmacokinetics in intravenous use.
Strength Variant Amoxicillin Content (as Sodium) Clavulanic Acid Content (as Potassium) Target Patient 1.2 g Vial 1000 mg (1 g) 200 mg Adults (Severe) 600 mg Vial 500 mg 100 mg Adults / Children 300 mg Vial 250 mg 50 mg Pediatric 150 mg Vial 125 mg 25 mg Infants *Pack Sizes: Tray of 1 Vial or Box of 1/10 Vials with Water for Injection (WFI).
Amoxycillin Capsules
FreeAmoxycillin capsules are widely used penicillin-type antibiotics. They are most frequently prescribed in 250 mg and 500 mg strengths.Amoxycillin Dispersible Kid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Fruit-Flavored Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive API.
Active Ingredient Strength Primary Clinical Function Amoxycillin (as Trihydrate) USP/BP 125 mg The Pediatric Starter: Ideal for infants and toddlers requiring low-dose respiratory or ear infection therapy. Amoxycillin (as Trihydrate) USP/BP 250 mg The Junior Anchor: The standard dose for older children and adolescents for broad-spectrum anti-infective coverage. Excipients Sweetened Matrix Taste-Masking System: Engineered with pleasant flavors (Strawberry/Pineapple/Orange) to overcome the natural bitterness of the antibiotic. Ampicillin & Cloxacillin Capsules
FreeAmpicillin and cloxacillin capsules (often called co-ampiclox) are combination antibiotics used to treat infections where the bacteria may produce enzymes that destroy standard penicillin. They are most commonly available in a 500 mg total strength (250 mg / 250 mg)
Ampicillin & Cloxacillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard 1:1 Ratio) Therapeutic Role Ampicillin Sodium USP/BP 250 mg Broad Spectrum Coverage Cloxacillin Sodium USP/BP 250 mg Anti-Staphylococcal Shield Total Vial Strength 500 mg Pediatric / Mild Infection (Adult Variant) 500 mg Ampicillin + 500 mg Cloxacillin (1 g Total) Standard Adult Dose Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ampicillin & Dicloxacillin Capsules
FreeAmpicillin and dicloxacillin capsules are combination antibiotics designed to provide broad-spectrum coverage while resisting degradation by certain bacterial enzymes. They are commonly available in a 500 mg total strength (typically 250 mg / 250 mg).
Ampicillin and Flucloxacillin Capsules
FreeAmpicillin and flucloxacillin capsules (often referred to by the co-drug name co-fluampicil) are combination antibiotics used to treat infections where the specific bacteria is unknown or suspected to be a penicillin-resistant strain. They are typically available in a 250 mg/250 mg strength.
Ampicillin Capsules
FreeAmpicillin capsules are a penicillin-type antibiotic used to treat various bacterial infections. They are most commonly available in 250 mg and 500 mg strengths.
Ampicillin Injection 1gm
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard Adult Dose) Therapeutic Role Ampicillin Sodium USP/BP Equivalent to 1000 mg (1 g) Ampicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ampicillin Injection 500mg
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard Pediatric/Mild Dose) Therapeutic Role Ampicillin Sodium USP/BP Equivalent to 500 mg Ampicillin Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ampicillin Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The 2:1 ratio is clinically optimized for pharmacokinetics.
Active Ingredient Strength (Standard 1.5g Vial) Strength (High Dose 3g Vial) Ampicillin Sodium USP/BP 1000 mg (1 g) 2000 mg (2 g) Sulbactam Sodium USP/BP 500 mg (0.5 g) 1000 mg (1 g) Total Vial Content 1.5 g 3.0 g Excipients None (Pure Sterile Powder) None (Pure Sterile Powder) *Pack Sizes: Tray of 10 Vials, or Box of 1 Vial with Water for Injection (WFI).
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. Antacid & Anti-Ulcerant Tablets
FreeTechnical & Logistics Specifications
Parameter Specifications & Standards HS Code 3004.90.99 (Medicaments acting on the alimentary tract and metabolism) Pharmacopeia Compliance IP / BP / USP / EP Dosage Formats Enteric-Coated, Delayed-Release, Film-Coated, and Chewable Tablets Export Packaging 10 / 14 / 15 Tablets per Blister packed exclusively in high-barrier Alu-Alu (Cold-Form Foil) or thick PVC/PVDC matrixes to protect against moisture ingress in Zone IVb tropical climates. Shelf-Life Stability Fully validated 36-Month real-time stability metrics 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. Aripipralzole Tablets
FreeProduct Composition & Strength
We supply this product in a wide range of strengths to allow for precise clinical titration, packed in moisture-resistant Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Aripiprazole USP/Ph.Eur. 2 mg / 5 mg The Titration/Adjunct Unit: Used for initial dosing or as an add-on for Major Depressive Disorder. Aripiprazole USP/Ph.Eur. 10 mg / 15 mg The Standard Anchor: The primary maintenance dose for Schizophrenia and Bipolar Disorder. Aripiprazole USP/Ph.Eur. 20 mg / 30 mg The High-Potency Payload: For acute manic episodes or treatment-resistant cases under specialist care Arteether Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules. The oily base (refined Arachis Oil or Ethyl Oleate) ensures depot formation in the muscle.
Active Ingredient Strength (Standard) Therapeutic Role α-β Arteether 150 mg / 2 ml Adult Dose (Standard) α-β Arteether 75 mg / 1 ml Pediatric Dose Vehicle Q.S. Refined Arachis Oil / Ethyl Oleate Oily Base (Sustained Release) *Pack Sizes: Tray of 3 Ampoules (Full Course) or Box of 10 Ampoules.
Artemether & Lumefantrine Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Yellow) or Dispersible Tablets (Sweetened for Pediatrics). The standard regimen is a fixed ratio of 1:6.
Strength Variant Artemether Content Lumefantrine Content Target Patient Standard / Pediatric 20 mg 120 mg Infants & Children (5kg–35kg) Double Strength (DS) 40 mg 240 mg Adolescents / Simplified Dosing Adult Forte (80/480) 80 mg 480 mg Adults (>35kg) – High Compliance Artemether 40mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules. The oily base ensures a depot effect for sustained release.
Active Ingredient Strength (Standard) Therapeutic Role Artemether IP/Ph.Int 40 mg / 1 ml Pediatric / Low Body Weight Dose Artemether IP/Ph.Int 80 mg / 1 ml Adult Standard Dose Vehicle Q.S. Refined Arachis Oil / Ethyl Oleate Oily Base (Depot) *Pack Sizes: Tray of 6 Ampoules or 10 Ampoules (Standard Course).
Artemether-80 Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules. The 80mg strength is specifically formulated to minimize the injection volume for adult patients while delivering a potent therapeutic dose.
Active Ingredient Strength (Adult Dose) Therapeutic Role Artemether IP/Ph.Int 80 mg Potent Antimalarial Vehicle Q.S. to 1 ml Refined Arachis Oil / Ethyl Oleate *Pack Sizes: Tray of 6 Ampoules or 10 Ampoules (Standard Adult Course).
Artesunate & Sulphadoxine-Pyrimethamine Tablets
FreeProduct Composition & Kit Configuration
We supply this product in standardized, age-titrated Fixed-Dose Combination (FDC) Blister Strips, commonly containing a 3-day course of Artesunate tablets alongside a single-dose treatment of Sulfadoxine-Pyrimethamine.
Component Tablet Type Active Ingredient Mix Standard Strengths (per Tablet) Primary Clinical Function Artesunate Tablet Artesunate 50 mg / 100 mg / 200 mg The Fast Cleaver: Clears parasite biomass over 3 consecutive days. Sulfadoxine-Pyrimethamine Tablet Sulfadoxine + Pyrimethamine 500 mg + 25 mg The Extended Shield: Single-dose companion to prevent recrudescence. Artesunate 120mg Injection
FreeProduct Composition & Strength
We supply this product as a Combi-Pack containing the Lyophilized Powder and special solvents required for activation.
Component Content Function Vial (Powder) Artesunate 120 mg (Sterile Lyophilized) Active Antimalarial Ampoule 1 Sodium Bicarbonate Injection (5%) – 1ml Activator / Solvent (Solubilizes the acid) Ampoule 2 Sodium Chloride Injection (0.9%) – 5ml Diluent (Adjusts volume/tonicity) *Pack Sizes: Single Combi-Pack or Tray of 5 Combi-Packs.
Artesunate 30mg Injection
FreeProduct Composition & Strength
We supply this product as a Combi-Pack containing the Lyophilized Powder and special solvents required for activation.
Component Content Function Vial (Powder) Artesunate 30 mg (Sterile Lyophilized) Active Antimalarial Ampoule 1 Sodium Bicarbonate Injection (5%) – 0.5ml Activator (Solubilizes the acid) Ampoule 2 Sodium Chloride Injection (0.9%) – 2.5ml Diluent (Adjusts volume/tonicity) *Pack Sizes: Single Combi-Pack or Tray of 5/10 Combi-Packs.
Artesunate 60mg Injection
FreeProduct Composition & Strength
We supply this product as a Combi-Pack containing the Lyophilized Powder and special solvents required for activation.
Component Content Function Vial (Powder) Artesunate 60 mg (Sterile Lyophilized) Active Antimalarial Ampoule 1 Sodium Bicarbonate Injection (5%) – 0.5ml/1ml Activator (Solubilizes the acid) Ampoule 2 Sodium Chloride Injection (0.9%) – 2.5ml/5ml Diluent (Adjusts volume/tonicity) *Pack Sizes: Single Combi-Pack or Tray of 5 Combi-Packs.
Artesunate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. Stability is a key factor in our formulation.
Active Ingredient Strength (Standard) Role Artesunate IP/BP 50 mg Pediatric / Initial Dose Artesunate IP/BP 100 mg Adult Standard Dose Artesunate IP/BP 200 mg High Strength (Combination Protocols) Ascorbic Acid Tablet
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (Sugar/Sugar-Free) or Film Coated Tablets (Swallowable).
Active Ingredient Strength (Standard) Form Role Ascorbic Acid IP/BP/USP 100 mg Uncoated / Coated Pediatric / Maintenance Ascorbic Acid IP/BP/USP 500 mg Chewable (Orange) Standard Adult Dose Ascorbic Acid IP/BP/USP 1000 mg Chewable / Effervescent High Potency / Immunity Sodium Ascorbate Var. Buffered Salt Reduced Acidity Variant Aspirin Tablets
FreeProduct Composition & Strength
We supply this product in various formats, including Gastro-resistant (Enteric-coated), Dispersible, and standard Film-coated tablets.
Active Ingredient Strength Primary Clinical Function Aspirin (Acetylsalicylic Acid) 75 mg / 81 mg The Cardiac Shield: Low-dose daily therapy for the prevention of heart attack and stroke. Aspirin (Acetylsalicylic Acid) 150 mg Post-Surgical Maintenance: Used for patients with stents or high-risk vascular profiles. Aspirin (Acetylsalicylic Acid) 300 mg / 500 mg The Analgesic Anchor: High-dose relief for acute pain, migraine, and rheumatic fever. 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 Atenolol & Indapamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, engineered for synchronized 24-hour hemodynamic control.
Active Ingredient Strength Primary Clinical Function Atenolol USP/BP 50 mg The Heart Rate Regulator: Controls cardiac output and myocardial oxygen demand. Indapamide USP/BP 2.5 mg The Metabolic-Neutral Diuretic: Reduces blood volume and provides direct vascular relaxation. Excipients Proprietary Matrix Steady-State Release System: Engineered to ensure consistent plasma concentrations of both drugs to prevent “dips” in BP control. Atenolol & S-Amlodipine Besylate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, utilizing high-purity S-Amlodipine Besylate to ensure stability.
Active Ingredient Strength Primary Clinical Function Atenolol USP/BP 25 mg / 50 mg The Heart Rate Regulator: Controls the “Pump” by reducing heart rate and myocardial oxygen demand. S-Amlodipine (as Besylate) USP/BP 2.5 mg / 5 mg The Vessel Relaxant: Pure chiral isomer for maximum vasodilation with minimum side effects (edema). Excipients Proprietary Matrix Chiral-Stability System: Engineered to ensure the S-enantiomer remains stable and does not racemize during the shelf-life. Atenolol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (often scored for dosage adjustment).
Active Ingredient Strength (Standard) Role Atenolol IP/BP/USP 25 mg Low Dose / Renal Impairment Atenolol IP/BP/USP 50 mg Standard Adult Dose Atenolol IP/BP/USP 100 mg High Potency / Angina Excipients Q.S. Binder / Disintegrant Atorvastatin & Aspirin and Clopidogrel Tablets
FreeProduct Composition & Strength
We supply this product typically in a Capsule-in-Capsule or Multi-Particulate Tablet format to ensure the chemical stability of the three distinct APIs.
Active Ingredient Strength Primary Clinical Function Atorvastatin (as Calcium) USP 10 mg / 20 mg The Lipid Stabilizer: Lowers cholesterol and prevents the growth of arterial blockages. Aspirin (Gastro-resistant) BP 75 mg / 150 mg The Primary Blood Thinner: Prevents initial platelet activation via the COX pathway. Clopidogrel (as Bisulphate) USP 75 mg The Secondary Blood Thinner: Provides high-level protection against stent thrombosis and recurrent stroke. Atorvastatin & Asprin Tablets
FreeProduct Composition & Strength
We supply this product as a Bi-Layered or Film-Coated Tablet, often utilizing specialized enteric coating for the Aspirin component to protect the stomach lining.
Active Ingredient Strength Primary Clinical Function Atorvastatin Calcium USP/BP 10 mg / 20 mg The Lipid Regulator: Controls cholesterol synthesis in the liver and stabilizes arterial walls. Aspirin (Gastro-resistant) BP 75 mg / 150 mg The Anti-Platelet Anchor: Provides low-dose blood thinning to prevent clot formation. Excipients Proprietary Matrix Gastro-Protective System: Engineered to ensure Aspirin dissolves only in the small intestine, minimizing gastric irritation. Atorvastatin Clopidogrel and Aspirin Capsules
FreeAtorvastatin, clopidogrel, and aspirin capsules are fixed-dose combination (FDC) medications used for the secondary prevention of cardiovascular events like heart attacks and strokes.
Atorvastatin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The active ingredient is used in the amorphous or crystalline form depending on bioavailability requirements.
Active Ingredient Strength (Standard) Role Atorvastatin Calcium IP/BP/USP 10 mg Primary Prevention / Maintenance Atorvastatin Calcium IP/BP/USP 20 mg Standard Therapeutic Dose Atorvastatin Calcium IP/BP/USP 40 mg High Intensity Therapy Atorvastatin Calcium IP/BP/USP 80 mg Acute Coronary Syndrome Atropine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Clear Glass Ampoules.
Active Ingredient Strength (Standard) Therapeutic Role Atropine Sulphate USP/BP 0.6 mg / ml Pre-operative / Cardiac Dose Atropine Sulphate USP/BP 1 mg / ml Emergency / Antidote Dose Excipients Q.S. Sodium Chloride / Sulfuric Acid (pH adjustment) Isotonicity / Stabilizer *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules (Hospital/Military Pack).
Azathioprine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Yellow/Pale Yellow) in blister packs or bulk containers.
Active Ingredient Strength (Standard) Role Azathioprine USP/BP 50 mg Standard Adult Dose Azathioprine USP/BP 25 mg Low Dose / Renal Adjustment Excipients Q.S. Binder / Coating Agent 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. Azithromycin & Cefixime tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, packed in high-barrier Alu-Alu blister strips to prevent the degradation of the moisture-sensitive API.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/BP 200 mg The Gram-Negative Specialist: Targets the cell walls of stubborn bacteria, highly effective in Typhoid and Bronchitis. Azithromycin (as Dihydrate) USP/BP 250 mg / 500 mg The Tissue-Penetrating Anchor: Provides prolonged activity in the lungs and soft tissues to eliminate intracellular pathogens. Excipients Proprietary Matrix Dual-Release System: Engineered to ensure synchronized absorption of both antibiotics despite their different chemical solubilities. Azithromycin Dispersible Tablet
FreeProduct Composition & Strength
We supply this product as Dispersible Tablets (DT) with advanced taste-masking technology.
Active Ingredient Strength Flavor Profile Role Azithromycin IP/BP/USP 100 mg Orange / Peppermint Pediatric Low Dose Azithromycin IP/BP/USP 250 mg Orange / Peppermint Pediatric Standard / Adult Excipients Q.S. Sweeteners Disintegrant / Flavor Azithromycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Infusion in glass vials. It must be reconstituted and further diluted before administration.
Active Ingredient Strength (Standard Adult Dose) Therapeutic Role Azithromycin (as Dihydrate/Citrate) Equivalent to 500 mg Azithromycin Broad Spectrum Macrolide Excipients Q.S. Citric Acid / Sodium Hydroxide pH Adjuster / Solubilizer *Pack Sizes: Tray of 1 Vial, 5 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Azithromycin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential to mask the extremely bitter taste and facilitate swallowing.
Active Ingredient Strength (Standard) Standard Regimen Primary Role Azithromycin Dihydrate USP/BP 250 mg 6 Tablets (3-5 Days) Step-down Therapy / Pediatric Azithromycin Dihydrate USP/BP 500 mg 3 Tablets (3 Days) Respiratory Infections / Typhoid Azithromycin Dihydrate USP/BP 1000 mg (1 g) 1 Tablet (Single Dose) STI (Chlamydia / Gonorrhea) Excipients Q.S. Pregelatinized Starch / HPMC Disintegration / Coating 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. Benfotiamine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in high-barrier Alu-Alu or Alu-PVC blister strips.
Active Ingredient Strength Primary Clinical Function Benfotiamine USP/Ph.Eur. 100 mg / 150 mg The Neuropathy Anchor: Standard daily dose for the prevention of diabetic complications and nerve maintenance. Benfotiamine USP/Ph.Eur. 300 mg The Therapeutic Max-Payload: High-potency dose for clinical management of established Peripheral Neuropathy and Retinopathy. Excipients Proprietary Matrix Lipid-Enhanced System: Engineered to ensure maximum intestinal uptake and stable plasma concentrations. Benzathine Penicillin Injection 1.2 MIU
FreeProduct Composition & Strength
We supply this product as a Sterile Powder for Suspension in glass vials. It requires reconstitution with Sterile Water for Injection to form a milky white suspension.
Active Ingredient Strength (International Units) Therapeutic Role Benzathine Penicillin G USP/BP 1,200,000 IU (1.2 MIU) Standard Adult Prophylaxis Excipients Q.S. Lecithin / Sodium Citrate Suspending / Buffering Agents *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Benzathine Penicillin Injection 2.4 MIU
FreeProduct Composition & Strength
We supply this product as a Sterile Powder for Suspension in glass vials. It requires reconstitution with Sterile Water for Injection to form a milky white suspension.
Active Ingredient Strength (International Units) Therapeutic Role Benzathine Penicillin G 1,200,000 IU (1.2 MIU) Pediatric / Standard Dose Benzathine Penicillin G 2,400,000 IU (2.4 MIU) Adult Syphilis / High Dose Benzathine Penicillin G 600,000 IU (0.6 MIU) Pediatric Prophylaxis Excipients Q.S. Lecithin / Sodium Citrate Suspending / Buffering Agents *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Benzhexol Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets. The chemical name Benzhexol and Trihexyphenidyl refer to the exact same molecule.
Active Ingredient Strength (Standard) Role Trihexyphenidyl HCl (Benzhexol) 2 mg Initial Dose / Mild EPS Trihexyphenidyl HCl (Benzhexol) 5 mg Forte / Maintenance Dose Excipients Q.S. Binder / Filler Benzthiazide & Triamterene Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Disintegration Tablet, packed in high-barrier Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Benzthiazide USP/BP 25 mg The Thiazide Payload: The primary driver for sodium and water excretion to lower blood pressure. Triamterene USP/BP 50 mg The Potassium Guardian: Physically prevents the loss of Potassium (K+) during the diuretic process. Excipients Proprietary Matrix Bio-Balance System: Engineered to ensure synchronized dissolution of both active APIs for maximum clinical synergy. Benzyl Penicillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Buffered Powder for Injection in glass vials. The potency is measured in International Units (IU).
Active Ingredient Strength (IU) Mass Equivalent Therapeutic Role Benzyl Penicillin Sodium 1,000,000 IU (1 MU) ~600 mg Standard Dose Benzyl Penicillin Sodium 5,000,000 IU (5 MU) ~3000 mg High Dose (Meningitis) Benzyl Penicillin Sodium 10,000,000 IU (10 MU) ~6000 mg Severe Sepsis Buffering Agent Sodium Citrate – pH Stabilizer *Pack Sizes: Tray of 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
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. Betamethasone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Clear Glass Ampoules. The phosphate ester ensures high water solubility and rapid onset of action.
Active Ingredient Strength (Standard) Therapeutic Role Betamethasone Sodium Phosphate USP/BP Equivalent to 4 mg Betamethasone Potent Anti-inflammatory Excipients Q.S. Disodium Edetate / Sodium Metabisulfite Stabilizer / Antioxidant *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules (Hospital Pack)
Betamethasone injection
FreeComposition
Betamethasone sodium Phosphate eq. to
betamethasone 4mg + Phenol IP 0.5%w/v
( As preservative) + WFI IP q.s injection
Each ml contains –
Betamethasone sodium Phosphate eq. to
betamethasone 4mg + Phenol IP 0.5%w/v
( As preservative) + WFI IP q.s
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
Betamethasone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Soluble Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive sodium phosphate salt.
Active Ingredient Strength Primary Clinical Function Betamethasone Sodium Phosphate BP/USP 0.5 mg The Maintenance Anchor: Standard dose for chronic inflammatory conditions and pediatric allergy management. Betamethasone Sodium Phosphate BP/USP 1 mg (Forte) The Crisis Payload: High-potency therapeutic dose for acute asthma, severe eczema, and drug reactions. Excipients Proprietary Matrix Instant-Dispersible System: Engineered to dissolve in seconds, ensuring maximum bioavailability and ease of administration. 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. Betnesol forte 1mg Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Soluble Tablet, packed in high-barrier Alu-Alu blister strips to ensure the stability of the moisture-sensitive sodium phosphate salt.
Active Ingredient Strength Primary Clinical Function Betamethasone Sodium Phosphate BP/USP 1 mg The Crisis Anchor: High-potency therapeutic dose for short-term management of acute asthma, severe eczema, and drug reactions. Excipients Proprietary Matrix Instant-Dispersible System: Engineered to dissolve in seconds, ensuring maximum bioavailability and ease of administration for all age groups 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. Biotin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed, High-Bioavailability Tablet, packed in moisture-resistant Alu-PVC or Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Biotin USP/BP (Vitamin H) 5 mg The Standard Maintenance Unit: The definitive therapeutic dose for treating brittle nails and mild hair thinning. Biotin USP/BP (Vitamin H) 10 mg The Therapeutic Max-Payload: High-potency dose utilized for severe deficiency, advanced dermatology protocols, and metabolic support. Excipients Proprietary Matrix Rapid-Release System: Engineered to ensure 100% water solubility for immediate intestinal absorption. Biperiden Tablets
FreeProduct Composition & Strength
We supply this product as Tablets (usually White, scored). The 2 mg strength is the global standard for titration.
Active Ingredient Strength (Standard) Primary Role Biperiden Hydrochloride USP/BP 2 mg Standard Therapeutic Dose Excipients Q.S. Lactose Monohydrate / Maize Starch Filler / Binder Bisacodyl Tablets
FreeProduct Composition & Strength
We supply this product as Enteric Coated Tablets (Gastro-resistant). The specialized coating is non-negotiable to prevent gastric irritation.
Active Ingredient Strength (Standard) Formulation Type Primary Role Bisacodyl USP/BP 5 mg Enteric Coated (Sugar or Film) Standard Adult Dose Bisacodyl USP/BP 10 mg Enteric Coated Strong Dose / Bowel Prep Excipients Q.S. Methacrylic Acid Copolymer (Enteric) pH-Dependent Release Bisoprolol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (distinctively shaped/scored). The low-dose range is critical for the “Start Low, Go Slow” titration required in heart failure.
Active Ingredient Strength (Standard) Shape/Color Primary Role Bisoprolol Fumarate USP/BP 2.5 mg White (Scored) Heart Failure Initiation Bisoprolol Fumarate USP/BP 5 mg Yellow/Pink (Scored) Standard Hypertension Bisoprolol Fumarate USP/BP 10 mg Orange/White High Dose Maintenance Excipients Q.S. Microcrystalline Cellulose / Hypromellose Filler / Coating Bleomycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder in glass vials. Potency is measured in USP Units, not milligrams.
Active Ingredient Strength Therapeutic Role Bleomycin Sulphate USP/IP 15 Units (approx. 15 mg) Antineoplastic Antibiotic Excipients Nitrogen (Inert Atmosphere) None (Pure Powder) *Pack Sizes: Single Vial Box or Tray of 10 Vials.
Bortenat
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder in glass vials. It must be reconstituted with Normal Saline (0.9% NaCl).
Active Ingredient Strength Reference Brand Bortezomib (as Mannitol Ester) 2 mg / Vial Bortenat 2mg Bortezomib (as Mannitol Ester) 3.5 mg / Vial Bortenat 3.5mg Excipients Mannitol USP/BP Stabilizer *Pack Sizes: Single Vial Box with protective Cytotoxic shrink-wrapping.
Bortezomib Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder in glass vials. It contains Mannitol, which forms a stable boronic ester with Bortezomib for shelf stability.
Active Ingredient Vial Strength Primary Use Bortezomib (as Mannitol Boronic Ester) 2 mg / Vial Single Dose / Low BSA Bortezomib (as Mannitol Boronic Ester) 3.5 mg / Vial Standard Adult Dose Excipients Mannitol (Sterile) Stabilizer / Bulking Agent *Pack Sizes: Single Vial Box with protective Cytotoxic shrink-wrapping.
ortezomib injection is an antineoplastic (cancer) medication supplied as a sterile lyophilised powder (freeze-dried cake) for reconstitution. It is most commonly known by the brand name Velcade.
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. Bromocriptin Tablets
FreeBromocriptin Mesylate Tablets IP 2.5 MG
Each uncoated tablet contains
Bromocriptin Mesylate IP
eq.to Bromocriptine 2.5 mgUsage: – high levels of a natural substance prolactin in the body
Category: – Anti Parkinson drugs
Therapeutic category: – Anti Parkinson
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.
Buprenorphine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed Sublingual Tablet, engineered for rapid mucosal absorption.
Active Ingredient Strength Primary Clinical Function Buprenorphine HCl USP/Ph.Eur. 0.4 mg / 2 mg The Pain & Induction Anchor: Low-dose format for chronic pain or the initial phase of addiction treatment. Buprenorphine HCl USP/Ph.Eur. 8 mg The Maintenance Payload: High-strength dose for long-term stabilization in Opioid Use Disorder. Excipients Sublingual Matrix Rapid Dissolution System: Engineered to dissolve completely under the tongue in < 2 minutes for maximum transmucosal bioavailability. Bupropion tablets
FreeProduct Composition & Strength
We supply this product in three distinct Release Profiles, packed in moisture-resistant Alu-Alu or HDPE containers to protect the stability of the hydrochloride salt.
Release Profile Strength Primary Clinical Function Bupropion XL (Extended Release) 150 mg / 300 mg The Depression Anchor: Once-daily dosing (24-hour release) for MDD and Seasonal Affective Disorder. Bupropion SR (Sustained Release) 150 mg The Smoking Cessation Specialist: Twice-daily dosing (12-hour release) for smoking cessation and MDD. Bupropion IR (Immediate Release) 75 mg / 100 mg The Titration Unit: Immediate-release format for precise dose escalation under specialist supervision. Cabergoline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed, Micro-Dose Tablet, packed in high-barrier Alu-Alu blister strips or specialized glass vials to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Cabergoline USP/Ph.Eur. 0.5 mg The Standard Specialty Anchor: The definitive therapeutic unit for managing prolactin-related infertility and pituitary tumors. Excipients Proprietary Matrix Micro-Gram Content Uniformity: Engineered utilizing Geometric Dilution techniques to ensure every 0.5 mg tablet contains the exact clinical dose across the entire batch. Calcium & Calcitriol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Softgel or Tablet, packed in high-barrier Alu-Alu or Blister strips to protect the light-sensitive Calcitriol.
Active Ingredient Strength Primary Clinical Function Calcium Carbonate USP/BP 500 mg (200 mg Elemental) The Mineral Substrate: Provides the high-density elemental calcium needed for skeletal reinforcement. Calcitriol USP/BP 0.25 mcg The Active Hormone: The potent, pre-activated Vitamin D that drives 100% absorption efficiency. Excipients Oil-Based Matrix Softgel Stability: For softgel formats, we utilize a specialized oil-base to ensure the fat-soluble Calcitriol remains fully dissolved and bioavailable. Calcium & Chloecalciferol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Swallowable) or Chewable Tablets (Flavor masked). The chewable format is popular due to the large size of calcium tablets.
Component Strength (Standard) Strength (High Potency) Role Elemental Calcium
(from Calcium Carbonate)500 mg
(1250 mg Salt)500 mg
(1250 mg Salt)Bone Mineralization Vitamin D3
(Cholecalciferol)250 IU 500 IU / 1000 IU Absorption Enhancer Excipients Q.S. Starch / Povidone Binding Agent Calcium Acetate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Disintegration Tablet, packed in moisture-resistant Alu-Alu or HDPE bottles.
Active Ingredient Strength Primary Clinical Function Calcium Acetate USP/Ph.Eur. 667 mg The Dialysis Anchor: Each 667mg tablet provides 169mg of elemental calcium, the standardized dose for maximum phosphate binding. Excipients Proprietary Matrix Rapid Dissolution System: Engineered to ensure the tablet shatters instantly in the stomach to maximize contact with dietary phosphorus during a meal. Calcium Carbonate & Vitamin D3 Tablets
FreeProduct Composition & Common Strengths
We supply this combination in standard, clinically calibrated ratios designed to optimize daily absorption thresholds without overwhelming intestinal transit.
Active Ingredient Components Standard Strengths (per Tablet) Elemental Yield / Biological Activity Primary Clinical Function Calcium Carbonate IP / BP / USP 1250 mg Yields 500 mg Elemental Calcium The Scaffold: Provides the physical structural block for bone density. Vitamin D3 (Cholecalciferol) IP/BP/USP 250 IU / 400 IU Equivalent to 6.25 mcg / 10.0 mcg The Catalyst: Chemically drives intestinal transport channels. Excipients Pharma Grade Modified Matrix Adjusters The Carrier: Ensures fast disintegration or chewable palatability. Calcium Citrate With Vitamin D3 Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Off-White, Oblong/Caplet shape). The coating makes the large tablet easier to swallow.
Active Ingredient Strength (Standard) Therapeutic Role Calcium Citrate USP/BP 1000 mg (Eq. to 210 mg Elemental Ca) Bone Mineralization Vitamin D3 (Cholecalciferol) USP/BP 200 IU / 400 IU / 1000 IU Absorption Enhancer (High Strength Variant) 1200 mg Citrate + 1000 IU D3 Severe Osteoporosis Excipients Q.S. Starch / Magnesium Stearate / HPMC Disintegrant / Coating Calcium Citrate, Vitamin D3, Methylcobalamin, Folic Acid & Pyridoxine HCl Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Potency Tablet, packed in moisture-resistant Alu-Alu or Alu-PVC blister strips to protect the sensitive B-vitamins.
Active Ingredient Strength Primary Clinical Function Calcium Citrate USP/BP 1000 mg The Structural Payload: Provides elemental calcium for bone mineral density (BMD) restoration. Vitamin D3 (Cholecalciferol) IP 200 IU / 400 IU The Absorption Catalyst: Facilitates active intestinal transport of calcium. Methylcobalamin USP/JP 1500 mcg The Nerve Restorer: Active B12 for nerve fiber regeneration and red blood cell formation. Folic Acid USP/BP 1.5 mg The DNA/Heme Synthesis Anchor: Essential for cell division and lowering homocysteine. Pyridoxine HCl (Vit B6) USP 3 mg The Metabolic Co-factor: Supports neurotransmitter synthesis and protein metabolism. Calcium Citrate,Vitamin D3, Magnesium, Zinc Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Blue, Oblong). The coating masks the metallic taste of Zinc and Magnesium.
Active Ingredient Strength (Standard) Therapeutic Role Calcium Citrate USP/BP 1000 mg (Eq. to 210 mg Elemental Ca) Bone Mineralization Vitamin D3 (Cholecalciferol) 200 IU / 400 IU Absorption Enhancer Magnesium Hydroxide USP/BP 100 mg (Eq. to Elemental Mg) D3 Activation / Bone Structure Zinc Sulphate Monohydrate USP/BP 4 mg / 10 mg (Eq. to Elemental Zn) Collagen Synthesis Excipients Q.S. Croscarmellose Sodium / HPMC Disintegrant / Coating Calcium Dobesilate Capsules
FreeCalcium dobesilate capsules are vasoprotective medications primarily used to treat chronic venous insufficiency and diabetic retinopathy. They are most commonly available in a 500 mg strength
Calcium Gluconate Injection
FreeProduct Composition & Strength
We supply this product as a Supersaturated Sterile Solution in 10ml ampoules.
Active Ingredient Concentration Elemental Calcium Content Calcium Gluconate Monohydrate USP/BP 10% w/v (100 mg / ml) 0.465 mEq/ml (Approx 9 mg Ca++ / ml) Stabilizer Calcium D-Saccharate Prevents Crystallization *Pack Sizes: Tray of 10 Ampoules (10ml) or 50 Ampoules.
Calcium Gluconate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Chewable Tablets in bulk jars or blisters.
Active Ingredient Strength Elemental Calcium Role Calcium Gluconate IP/BP/USP 500 mg ~ 45 mg Pediatric / Maintenance Calcium Gluconate IP/BP/USP 1000 mg (1g) ~ 90 mg Adult Therapeutic Dose Excipients Q.S. — Binder / Sweetener Calcium Pantothanate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed, High-Purity Tablet, packed in moisture-resistant Alu-PVC or Alu-Alu blister strips to prevent the hygroscopic vitamin from degrading.
Active Ingredient Strength Primary Clinical Function D-Calcium Pantothenate USP/BP 50 mg / 100 mg The Wellness & Hair Anchor: Standard daily dose for nutritional support and maintenance of hair/skin health. D-Calcium Pantothenate USP/BP 250 mg / 500 mg The Therapeutic Payload: High-dose intervention for clinical B5 deficiency, acne management, and post-surgical wound healing. Excipients Proprietary Matrix Moisture-Lock Formulation: Engineered utilizing specialized binders to protect the vitamin from atmospheric humidity, ensuring a 36-year shelf life in Zone IVb tropical climates. 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. Candesartan Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). The wide range of strengths allows for precise titration in heart failure patients.
Active Ingredient Strength (Standard) Primary Role Candesartan Cilexetil USP/BP 4 mg Heart Failure Initiation / Hepatic Impairment Candesartan Cilexetil USP/BP 8 mg Standard Hypertension Start Candesartan Cilexetil USP/BP 16 mg Standard Maintenance Candesartan Cilexetil USP/BP 32 mg High Dose / Resistant Hypertension 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. Carbamazepine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (White, scored). We also offer Controlled Release (CR) variants upon request.
Active Ingredient Strength (Standard) Primary Role Carbamazepine USP/BP 100 mg Pediatric / Initiation Dose Carbamazepine USP/BP 200 mg Standard Adult Dose Carbamazepine USP/BP 400 mg High Dose / CR Formulation Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Carbidopa and Levodopa Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (often scored/mottled). The ratios are designed to minimize nausea while maximizing brain dopamine levels.
Carbidopa (Anhydrous) Levodopa Ratio Primary Role 10 mg 100 mg 1:10 Low Dose Initiation 25 mg 100 mg 1:4 Standard Maintenance (Best Nausea Control) 25 mg 250 mg 1:10 High Dose / Advanced Disease Excipients Q.S. Microcrystalline Cellulose / Starch / Dye Filler / Colorant Carbimazole Tablets
FreeProduct Composition & Available Strengths
We manufacture Carbimazole in exact, internationally recognized strengths to facilitate precise dosage titration based on periodic patient blood chemistry.
Active Ingredient Standard Strengths Primary Clinical Target Carbimazole BP/IP/USP 5 mg Maintenance Titration: For long-term control once stable thyroid levels are chemically achieved. Carbimazole BP/IP/USP 10 mg Initial Suppression: High-dose intervention to rapidly bring down severely elevated $T_{3}$/$T_{4}$ levels. Carboplatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid Concentrate in glass vials. It is ready to dilute.
Active Ingredient Concentration Vial Size (Total Drug) Carboplatin USP/BP 10 mg / ml 150 mg (15 ml vial) Carboplatin USP/BP 10 mg / ml 450 mg (45 ml vial) Excipients Water for Injection / Mannitol – *Pack Sizes: Single Vial Box with protective Cytotoxic shrink-wrapping.
Carvedilol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. Because therapy for Heart Failure requires very precise “low dose” initiation, we offer the full titration range.
Active Ingredient Strength (Standard) Color Code (Typical) Role Carvedilol USP/BP 3.125 mg White/Pink CHF Initiation (Critical) Carvedilol USP/BP 6.25 mg Yellow Titration Step 1 Carvedilol USP/BP 12.5 mg Tan/Peach Titration Step 2 Carvedilol USP/BP 25 mg White Target Maintenance Dose Cefadroxil 500 mg Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant Alu-Alu or High-Density Alu-PVC blister strips to ensure the absolute stability of the beta-lactam ring.
Active Ingredient Strength Primary Clinical Function Cefadroxil Monohydrate USP/Ph.Eur. 500 mg (Equivalent to anhydrous Cefadroxil) Global Standard: Twice-daily adult therapy for pharyngitis, skin infections, and UTIs. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Macrogol / Magnesium Stearate Diluent / Superdisintegrant / Film-Coating (Engineered for rapid gastric dissolution and high bioavailability) Cefadroxil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Monohydrate Tablet, packed in high-barrier Alu-PVC or Alu-Alu blister strips to ensure the stability of the active API.
Active Ingredient Strength Primary Clinical Function Cefadroxil (as Monohydrate) USP/Ph.Eur. 250 mg The Pediatric & ENT Anchor: Ideal for Pharyngitis, Tonsillitis, and mild skin infections in adolescents. Cefadroxil (as Monohydrate) USP/Ph.Eur. 500 mg The Dermatology & UTI Payload: High-efficacy therapeutic dose for Cellulitis, Impetigo, and bladder infections. Excipients Proprietary Matrix High-Density Granulation: Engineered to manage the bulk of the 500mg payload while ensuring rapid disintegration and consistent absorption. Cefazolin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It must be reconstituted with Sterile Water for Injection prior to use.
Active Ingredient Strength (Standard) Therapeutic Role Cefazolin Sodium USP/BP Equivalent to 1000 mg (1 g) Cefazolin Adult Surgical Dose Cefazolin Sodium USP/BP Equivalent to 500 mg Cefazolin Pediatric / Mild Infection Excipients None (Pure Sterile Powder) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefdinir 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 ingredient.
Active Ingredient Strength Primary Clinical Function Cefdinir USP/Ph.Eur. 300 mg The Respiratory & Skin Anchor: The definitive therapeutic unit utilized for CAP, Sinusitis, and Skin/Soft Tissue Infections (SSTI). Excipients Proprietary Matrix Crystalline Form Stability: Engineered utilizing specialized binders to maintain the Crystalline Form I of Cefdinir, ensuring maximum shelf-life and predictable intestinal absorption. Cefepime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefepime Content Sulbactam Content Ratio 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) 2:1 (Standard) Excipients L-Arginine Buffer / Stabilizer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefepime Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients L-Arginine Buffer / Stabilizer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefepime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains L-Arginine as a buffering agent (instead of sodium salts).
Active Ingredient Strength Therapeutic Role Cefepime Hydrochloride USP/BP Equivalent to 1000 mg (1 g) Cefepime Severe Infection / Sepsis Cefepime Hydrochloride USP/BP Equivalent to 500 mg Cefepime Pediatric / Moderate Infection Buffer L-Arginine pH Stabilizer (Approx 725 mg per g) *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefixime & Potassium Clavulanate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Protected Tablet, packed exclusively in high-barrier Alu-Alu blister strips to ensure the stability of the highly sensitive Clavulanate payload.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/Ph.Eur. 200 mg The 3rd-Gen Payload: Broad-spectrum bactericidal activity targeting resistant Gram-negative bacilli and Enteric pathogens. Potassium Clavulanate Diluted BP/USP 125 mg The Beta-Lactamase Shield: Irreversibly inhibits the enzymes that cause antibiotic resistance. Excipients Proprietary Matrix Moisture-Scavenging Formulation: Engineered specifically utilizing Low-Humidity Processing (RH < 20%). Clavulanic acid is extremely hygroscopic; our tablets use special desiccant-compatible excipients to prevent degradation. Cefixime and Clavulanic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Protected Tablet, packed exclusively in high-barrier Alu-Alu blister strips to ensure the stability of the highly sensitive Clavulanate payload.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/Ph.Eur. 200 mg The 3rd-Gen Payload: Broad-spectrum bactericidal activity targeting resistant Gram-negative bacilli and Enteric pathogens. Potassium Clavulanate Diluted BP/USP 125 mg The Beta-Lactamase Shield: Irreversibly inhibits the enzymes that cause antibiotic resistance. Excipients Proprietary Matrix Moisture-Scavenging Formulation: Engineered specifically utilizing Low-Humidity Processing (RH < 20%). Clavulanic acid is extremely hygroscopic; our tablets use special desiccant-compatible excipients to prevent degradation. Cefixime and Linezolid 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 the stability of the moisture-sensitive APIs.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/Ph.Eur. 200 mg The Gram-Negative Anchor: Broad-spectrum bactericidal activity against H. influenzae, E. coli, and Salmonella. Linezolid USP/Ph.Eur. 600 mg The Gram-Positive Powerhouse: Bacteriostatic activity against multi-drug resistant Staphylococci and Streptococci. Excipients Proprietary Matrix Advanced Disintegration System: Engineered utilizing Super-Disintegrants to manage the large 800mg+ active payload, ensuring the tablet shatters rapidly for maximum absorption. Cefixime and Ofloxacin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bilayer or Co-Processed Tablet, packed in high-barrier Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/Ph.Eur. 200 mg The Extracellular Specialist: Targets the bacterial cell wall; highly effective against Gram-negative enteric pathogens. Ofloxacin USP/Ph.Eur. 200 mg The Intracellular Specialist: Targets DNA replication; excellent tissue penetration into the lungs, prostate, and urinary tract. Excipients Proprietary Matrix Bilayer Technology: Engineered to prevent physical interaction between the two APIs, ensuring maximum stability and a synchronized release profile in the gut. Cefixime Capsules 400mg
FreeCefixime 400mg capsules are third-generation cephalosporin antibiotics used for a variety of bacterial infections. While 200mg is a common dose, the 400mg strength is often used for once-daily dosing.
Cefixime Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapidly Disintegrating (DT) Matrix, packed in high-barrier Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Cefixime Trihydrate USP/Ph.Eur. 100 mg / 200 mg The Pediatric & Enteric Anchor: Dispersible format for easy administration in children and patients with dysphagia. Excipients Sweetening & Flavoring Agents Compliance Engineering: Formulated with high-grade fruit flavors and non-cariogenic sweeteners to mask the bitter antibiotic taste, ensuring 100% pediatric compliance. Disintegrants Super-Disintegrant Blend Instant-Dispersible Matrix: Engineered to shatter and form a smooth, grit-free suspension in < 45 seconds when placed in 5-10 mL of water. Cefixime Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed exclusively in high-barrier Alu-Alu blister strips to ensure the stability of the trihydrate salt.
Active Ingredient Strength Primary Clinical Function Cefixime (as Trihydrate) USP/Ph.Eur. 200 mg The Standard Primary Care Anchor: Utilized for uncomplicated UTIs, Otitis Media, and Pharyngitis. Cefixime (as Trihydrate) USP/Ph.Eur. 400 mg The Enteric & Gonorrhea Payload: High-efficacy therapeutic dose for Typhoid Fever and uncomplicated Gonorrhea. Excipients Proprietary Matrix Solubility Enhancement: Engineered utilizing Laser Micronization of the API to ensure rapid dissolution and 100% bioequivalence to the innovator brand. Cefoperazone & Sulbactam 2Gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in 20ml glass vials.
Active Ingredient Strength Function Cefoperazone Sodium USP/BP 1000 mg (1 g) Anti-Pseudomonal Cephalosporin Sulbactam Sodium USP/BP 1000 mg (1 g) Beta-Lactamase Inhibitor Ratio 1 : 1 High Sulbactam Load *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with 10ml Water for Injection (WFI).
Cefoperazone & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 1:1.
Strength Variant Cefoperazone Content Sulbactam Content Ratio 1.5 g Vial 500 mg (Sodium) 500 mg (Sodium) 1:1 (Standard) 3.0 g Vial 1000 mg (1 g) 1000 mg (1 g) 1:1 (High Dose) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefoperazone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefoperazone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – Cefoperazone Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approximately 34 mg (1.5 mEq) of sodium per gram.
Active Ingredient Strength (Standard) Therapeutic Role Cefoperazone Sodium USP/BP Equivalent to 1000 mg (1 g) Cefoperazone Adult Surgical / Biliary Dose Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefopodoxime Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Matrix, packed in high-barrier Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Cefpodoxime Proxetil USP/Ph.Eur. 100 mg The Pediatric & Titration Anchor: Ideal for Pharyngitis, Tonsillitis, and uncomplicated UTIs in adolescents and adults. Cefpodoxime Proxetil USP/Ph.Eur. 200 mg The Respiratory Macrodose: High-efficacy payload for Community-Acquired Pneumonia and Sinusitis. Excipients Proprietary Matrix Solubility Enhancement: Engineered utilizing micronized API and specialized surfactants to overcome the naturally poor solubility of the Proxetil salt. Cefotaxime Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The sodium content is lower than many other cephalosporins (approx 2.2 mmol/g).
Active Ingredient Strength Primary Patient Cefotaxime Sodium USP/BP Equivalent to 1000 mg (1 g) Adults (Meningitis/Sepsis) Cefotaxime Sodium USP/BP Equivalent to 500 mg Pediatrics Cefotaxime Sodium USP/BP Equivalent to 250 mg Neonates / Infants Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefpirome & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefpirome Content (as Sulfate) Sulbactam Content (as Sodium) Ratio 1.5 g Vial 1000 mg (1 g) 500 mg 2:1 (Standard) Excipients Sodium Carbonate Buffer – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefpirome Sulfate Injection
FreeCefpirome sulfate injection is a fourth-generation cephalosporin antibiotic typically supplied as a sterile dry powder for intravenous (IV) or intramuscular (IM) administration
Cefpodoxime & Clavulanic acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Protected Tablet, packed exclusively in high-barrier Alu-Alu blister strips to ensure the stability of the highly sensitive Clavulanate payload.
Active Ingredient Strength Primary Clinical Function Cefpodoxime Proxetil USP/Ph.Eur. 200 mg The 3rd-Gen Payload: Broad-spectrum bactericidal activity targeting resistant Gram-negative and Gram-positive pathogens. Potassium Clavulanate Diluted BP/USP 125 mg The Beta-Lactamase Shield: Irreversibly inhibits the enzymes that cause antibiotic resistance. Excipients Proprietary Matrix Moisture-Scavenging Formulation: Engineered specifically utilizing Low-Humidity Processing (RH < 20%). Clavulanic acid is extremely hygroscopic; our tablets use special desiccant-compatible excipients to prevent degradation. Cefpodoxime Proxetil Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapidly Disintegrating (DT) Matrix, packed in high-barrier Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Cefpodoxime Proxetil USP/Ph.Eur. 50 mg / 100 mg The Pediatric & Titration Anchor: Dispersible format for easy administration in children and elderly patients with swallowing difficulties. Excipients Sweetening & Flavoring Agents Bitter-Shield Technology: Engineered with molecular masking agents (e.g., Cyclodextrins) to neutralize the intense bitterness of the API, ensuring 100% pediatric compliance. Disintegrants Croscarmellose Sodium / SSG Instant-Dispersible Matrix: Engineered to shatter and form a uniform suspension in < 60 seconds when placed in 5-10 mL of water. Cefpodoxime-Potassium-Clavulanate-Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Protected Tablet, packed exclusively in high-barrier Alu-Alu blister strips to ensure the stability of the highly sensitive Clavulanate payload.
Active Ingredient Strength Primary Clinical Function Cefpodoxime Proxetil USP/Ph.Eur. 200 mg The 3rd-Gen Payload: Broad-spectrum bactericidal activity targeting resistant Gram-negative and Gram-positive pathogens. Potassium Clavulanate Diluted BP/USP 125 mg The Beta-Lactamase Shield: Irreversibly inhibits the enzymes that cause antibiotic resistance. Excipients Proprietary Matrix Moisture-Scavenging Formulation: Engineered specifically utilizing Low-Humidity Processing (RH < 20%). Clavulanic acid is extremely hygroscopic; our tablets use special desiccant-compatible excipients to prevent degradation. Cefprozil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Monohydrate Tablet, packed in high-barrier Alu-Alu blister strips to prevent hydrolytic degradation.
Active Ingredient Strength Primary Clinical Function Cefprozil USP/Ph.Eur. 250 mg The Pediatric & Mild Infection Anchor: Ideal for Pharyngitis, Tonsillitis, and mild skin infections. Cefprozil USP/Ph.Eur. 500 mg The Respiratory & SSTI Macrodose: Utilized for Acute Sinusitis, secondary infections of Bronchitis, and complicated skin infections. Excipients Proprietary Matrix Hydrolysis-Resistant Formulation: Engineered utilizing high-density granulation to protect the monohydrate API from environmental moisture. Ceftazidime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is either 2:1 or 1:1 depending on the market requirement.
Strength Variant Ceftazidime Content Sulbactam Content Ratio 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) 2:1 (Standard) 2.25 g Vial 1125 mg 1125 mg 1:1 (High Potency) Excipients Sodium Carbonate Buffer – *Pack Sizes: Tray of 1 Vial or Box of 1/10 Vials with Water for Injection (WFI).
Ceftazidime & Tazobactam Injection
FreeCeftazidime and tazobactam injection is a combination antibiotic used primarily in hospital settings for serious, multi-drug resistant bacterial infections. It is typically available as a sterile dry powder for reconstitution.
Product Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Ceftazidime Content Tazobactam Content Target Patient 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) Standard Adult Dose 281.25 mg Vial 250 mg 31.25 mg Pediatric Dose Excipients Sodium Carbonate Buffer Solubilizer Ceftazidime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains Sodium Carbonate as a solubilizer.
Active Ingredient Strength Primary Patient Ceftazidime Pentahydrate USP/BP Equivalent to 1000 mg (1 g) Adults (Standard Dose) Ceftazidime Pentahydrate USP/BP Equivalent to 250 mg Pediatrics / Neonates Excipients Sodium Carbonate Gas-Releasing Buffer *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftizoxime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approx. 2.6 mEq (60 mg) of sodium per gram.
Active Ingredient Strength Primary Use Ceftizoxime Sodium USP/BP Equivalent to 1000 mg (1 g) Ceftizoxime Severe Infection / Anaerobic Ceftizoxime Sodium USP/BP Equivalent to 500 mg UTI / Gonorrhea Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone & Sulbactam injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Ceftriaxone Content Sulbactam Content Target Patient 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) Adult Standard Dose 750 mg Vial 500 mg 250 mg Pediatric / Moderate Dose 375 mg Vial 250 mg 125 mg Infant / Neonate Dose Ratio 2 : 1 – Optimal Synergy *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone & Sulbactam veterinary injection
FreeCompotion
Ceftriaxone & Sulbactam VET INJ. 3 GM
Ceftriaxone & Sulbactam VET INJ. 4.5 GM
Usage: – used in veterinary medicine to treat bacterial infections in animals.
Category: – veterinary injection
Therapeutic category: –veterinary medicine
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
Ceftriaxone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Ceftriaxone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) 562.5 mg Vial 500 mg 62.5 mg Pediatric Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone 1gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Standard Use Ceftriaxone Sodium USP/BP Equivalent to 1000 mg (1 g) Ceftriaxone Adult Standard Dose Sodium Content Approx 83 mg (3.6 mEq) Per 1g Vial *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone 500mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Target Use Ceftriaxone Sodium USP/BP Equivalent to 500 mg Ceftriaxone Pediatrics / IM Gonorrhea Sodium Content Approx 41.5 mg (1.8 mEq) Low Sodium Load *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Ceftriaxone injection
FreeComposition
Cefotaxime Sodium 1000mg Vial+wfi
Ceftriaxone 1000mg Vial+wfi
Ceftriaxone 250mg Vial+wfi
Ceftriaxone 500mg Vial+wfi
Ceftriaxone 250mg & Sulbactam 125mg Vial+wfi
Ceftriaxon 1000mg & Sulbactam 500mg Vial+wfi
Ceftriaxone 1000mg & Tazobactam 125mg Vial+wfi
Usage: – It may be used for the treatment of complicated or severe urinary tract infections.
Category: – Ceftriaxone injection
Therapeutic category: –various bacterial infections
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
Cefuroxime & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 2:1.
Strength Variant Cefuroxime Content Sulbactam Content Primary Use 1.5 g Vial 1000 mg (1 g) 500 mg (Sodium) Adult Therapy / Surgery 1.125 g Vial 750 mg 375 mg Moderate Infection 375 mg Vial 250 mg 125 mg Pediatrics *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime Axetil Tablets
FreeProduct Composition & StrengthWe supply this product as a Precision-Blended, Amorphous Solid Dispersion Tablet, packed exclusively in secure, moisture-resistant Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Cefuroxime Axetil USP/Ph.Eur. 250 mg The Pediatric & ENT Anchor: Utilized for Acute Otitis Media, Pharyngitis, and uncomplicated UTIs. Cefuroxime Axetil USP/Ph.Eur. 500 mg The Respiratory Macrodose: Utilized for Community-Acquired Pneumonia, Bronchitis, and early-stage Lyme Disease. Excipients Proprietary Matrix Amorphous Solid Dispersion Technology: Engineered to maintain the API in its highly-soluble amorphous state for maximum clinical cure rates. Cefuroxime Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cefuroxime Sodium USP/BP Equivalent to 750 mg Cefuroxime Standard Adult Dose Cefuroxime Sodium USP/BP Equivalent to 1500 mg (1.5 g) Severe Infections / Surgery Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cefuroxime Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Amorphous Solid Dispersion Tablet, packed exclusively in secure, moisture-resistant Alu-Alu blister strips to ensure the stability of the hygroscopic prodrug.
Active Ingredient Strength Primary Clinical Function Cefuroxime Axetil USP/Ph.Eur.
(Equivalent to Cefuroxime)250 mg The Pediatric & ENT Anchor: The definitive unit utilized for the treatment of Acute Otitis Media, Pharyngitis, and uncomplicated Urinary Tract Infections. Cefuroxime Axetil USP/Ph.Eur. 500 mg The Respiratory Macrodose: The high-efficacy therapeutic payload required for the management of Community-Acquired Pneumonia, Bronchitis, and early-stage Lyme Disease. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Sodium Lauryl Sulfate / Colloidal Silicon Dioxide / Premium Polymeric Film Diluent / Superdisintegrant / Solubilizer / Glidant / Film-Coating (Engineered specifically utilizing Amorphous Solid Dispersion Technology. Because crystalline Cefuroxime Axetil has near-zero bioavailability, our tablets are engineered to maintain the API in its highly-soluble amorphous state for maximum clinical cure rates). *Pack Sizes: 1×6, 1×10, or 10×10 Alu-Alu Blisters (Optimized specifically for strict 5-to-10 day acute curative regimens).
Celecoxib Capsules
FreeCelecoxib capsules are selective non-steroidal anti-inflammatory drugs (NSAIDs) used to manage pain and inflammation. They are commonly available in strengths of 50 mg, 100 mg, 200 mg, and 400 mg.
Cephalexin Capsules
FreeCephalexin capsules are a first-generation cephalosporin antibiotic used to treat various bacterial infections. They are typically available in strengths of 250 mg, 500 mg, and sometimes 333 mg or 750 mg.
Cephalothin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. It contains approximately 2.8 mEq (64 mg) of Sodium per gram.
Active Ingredient Strength Therapeutic Role Cephalothin Sodium USP/BP Equivalent to 1000 mg (1 g) Cephalothin Surgical Prophylaxis / Skin Infection Excipients Sodium Bicarbonate Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cetrizine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (White/scored). The tablets are scored to facilitate dose splitting for pediatric use.
Active Ingredient Strength (Standard) Primary Role Cetirizine HCl USP/BP/IP 5 mg Pediatric / Mild Allergy Cetirizine HCl USP/BP/IP 10 mg Standard Adult Dose Excipients Q.S. Lactose Monohydrate / Maize Starch Chlorambucil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Dose Cytotoxic Tablet, packed exclusively in light-shielded, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the sensitive aromatic mustard payload.
Active Ingredient Strength Primary Clinical Function Chlorambucil USP/Ph.Eur. 2 mg The Standard Hematology Anchor: The definitive unit utilized for chronic, daily maintenance and precise titration in CLL and low-grade lymphomas. Chlorambucil USP/Ph.Eur. 5 mg The Pulse-Dosing Payload: High-efficacy therapeutic payload utilized for “Pulse” therapy regimens or initial aggressive induction phases. Excipients Lactose Anhydrous / Colloidal Silicon Dioxide / Magnesium Stearate / Hypromellose / Titanium Dioxide / Premium Polymeric Film Diluent / Glidant / Lubricant / Protective Cytotoxic Shield (Engineered specifically utilizing an impenetrable film coat. This ensures the highly toxic, mutagenic API never comes into contact with the skin of the pharmacist or caregiver handling the medication). *Pack Sizes: 25-Tablet or 30-Tablet Bottles/Blisters (Optimized for oncology-specific treatment cycles).
Chloramphenicol Capsules
FreeChloramphenicol capsules are broad-spectrum antibiotic medications primarily containing the active ingredient chloramphenicol. They are typically available in strengths of 250 mg or 500 mg per capsule.
Chloramphenicol Sodium Succinate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials. It must be reconstituted before use.
Active Ingredient Strength Therapeutic Role Chloramphenicol Sodium Succinate USP/BP Equivalent to 1000 mg (1 g) Chloramphenicol Broad Spectrum Antibiotic Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Chlordiazepoxide Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (often Green or Yellow). The robust coating is essential to mask the intensely bitter taste of the API and protect the light-sensitive drug.
Active Ingredient Strength (Standard) Therapeutic Role Chlordiazepoxide HCl USP/BP 10 mg Mild Anxiety / Elderly / Taper End Chlordiazepoxide HCl USP/BP 25 mg Severe Anxiety / Alcohol Detox Loading Excipients Q.S. Sucrose / Talc / Calcium Carbonate Sugar Coating (Light Barrier) Chloroquine Phosphate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Vials/Ampoules.
Active Ingredient Salt Strength Base Equivalent Chloroquine Phosphate USP/BP 64.5 mg / ml Equivalent to 40 mg Chloroquine Base Total Vial Content 30 ml Multi-dose Vial 1200 mg Base Total Excipients Chlorocresol (Preservative) Water for Injection *Pack Sizes: Tray of 10 Ampoules (5ml) or Multi-dose Vials (30ml).
Chloroquine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets or Uncoated Tablets. The strength is often labeled by the salt weight or the base equivalent.
Active Ingredient Salt Strength Base Equivalent (Active) Primary Role Chloroquine Phosphate USP/BP 250 mg 150 mg Base Pediatric / Prophylaxis Chloroquine Phosphate USP/BP 500 mg 300 mg Base Standard Adult Dose Excipients Q.S. Maize Starch / Magnesium Stearate Binder / Lubricant Chloroquine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is critical to mask the intensely bitter taste of the drug. Note: Dosing is often calculated based on the “Base” content.
Active Ingredient (Salt) Equivalent Base Primary Role Chloroquine Phosphate USP/BP 250 mg ~ 155 mg Base Prophylaxis / Maintenance Chloroquine Phosphate USP/BP 500 mg ~ 310 mg Base Acute Malaria Treatment Excipients Q.S. Starch / Magnesium Stearate Chlorphenamine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Therapeutic Role Chlorphenamine Maleate USP/BP 10 mg / ml Potent Antihistamine Excipients Sodium Chloride / Water for Injection Isotonicity Agent *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules (Hospital/ER Pack).
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).
Chlorpromazine Tablets
FreeProduct Composition & Available Strengths
We provide this therapeutic in a versatile range of strengths to allow for the precise dose titration required in specialized psychiatric medicine.
Active Ingredient Standard Strengths Primary Clinical Target Chlorpromazine HCl IP/BP/USP 25 mg Low-Dose Titration: For anxiety, pediatric hiccups, or elderly care. Chlorpromazine HCl IP/BP/USP 50 mg Maintenance Therapy: For stable outpatient management of schizophrenia. Chlorpromazine HCl IP/BP/USP 100 mg Acute Crisis Control: High-potency dosing for acute manic or psychotic states. Chlorthalidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed in moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the stability of the micronized active ingredient.
Active Ingredient Strength Primary Clinical Function Chlorthalidone USP/BP 6.25 mg / 12.5 mg The Contemporary Starting Dose: Highly preferred for modern “Low-Dose” hypertension therapy to maximize pressure control while minimizing electrolyte loss. Chlorthalidone USP/BP 25 mg The High-Potency Payload: Utilized for resistant hypertension or the management of edema associated with heart failure or hepatic cirrhosis. Excipients Microcrystalline Cellulose / Colloidal Silicon Dioxide / Magnesium Stearate / Pregelatinized Starch Diluent / Glidant / Lubricant / Binder (Engineered specifically utilizing Micronized API Technology to ensure absolute uniformity in the 6.25mg and 12.5mg ultra-low-dose tablets, guaranteeing consistent renal response across every batch). Chlorzoxazone ,Ibuprofen & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as a High-Density, Precision-Compressed Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the stability of the large multi-API payload.
Active Ingredient Strength Primary Clinical Function Chlorzoxazone USP/BP 250 mg The Muscle Relaxant Anchor: Targets the spinal cord to inhibit the reflexes driving the muscle spasm. Ibuprofen USP/BP 400 mg The Anti-Inflammatory Payload: Blocks prostaglandin synthesis to reduce tissue swelling and peripheral pain. Paracetamol (Acetaminophen) USP/BP 325 mg The Central Analgesic Booster: Synergistically raises the pain threshold for rapid symptomatic relief. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Magnesium Stearate / Polymeric Film Coat Diluent / Superdisintegrant / Binder / Lubricant (Engineered specifically utilizing High-Pressure Rotary Compression to manage the massive ~1000mg tablet weight while ensuring the tablet remains swallowable and shatters instantly in gastric fluid). *Pack Sizes: 10×10 Blisters (Optimized specifically for 5-day to 10-day acute injury recovery cycles).
Cholecalciferol (Vitamin D3) Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in glass ampoules.
Active Ingredient Strength Vehicle Cholecalciferol USP/BP (Vitamin D3) 300,000 IU / 1 ml (7.5 mg) Oily Base (Arachis or Sesame Oil) Cholecalciferol USP/BP (Vitamin D3) 600,000 IU / 1 ml (15 mg) Oily Base (Arachis or Sesame Oil) Excipients BHT / Benzyl Alcohol Antioxidant / Preservative *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Cholecalciferol Granules Sachet
FreeProduct Composition & Strength
We supply this product as Free-Flowing Granules in 1-gram sachets (Single Dose). The granules are flavored (Orange/Lemon) to ensure palatability.
Active Ingredient Strength Formulation Base Role Cholecalciferol (Vitamin D3) IP/BP/USP 60,000 IU Stabilized Powder Deficiency Correction Excipients Q.S. to 1 gm Sucrose / Mannitol / Flavor Diluent / Taste Masking 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). Cimetidine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Green or Blue). The coating masks the characteristic bitter taste and sulfur-like odor of the drug.
Active Ingredient Strength (Standard) Primary Role Cimetidine USP/BP 200 mg Prophylaxis / Maintenance Cimetidine USP/BP 400 mg Standard Therapeutic Dose Cimetidine USP/BP 800 mg Once-Daily (Bedtime) Excipients Q.S. Povidone / Magnesium Stearate CINITAPRIDE TABLETS
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Dose Gastric Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the hydrogen tartrate salt.
Active Ingredient Strength Primary Clinical Function Cinitapride Hydrogen Tartrate 1 mg The Global Prokinetic Anchor: The definitive therapeutic unit utilized to accelerate gastric emptying and increase esophageal tone in patients with chronic GERD or dyspepsia. Excipients Lactose Monohydrate / Maize Starch / Povidone K-30 / Magnesium Stearate / Hypromellose / Titanium Dioxide (Film Coat) Diluent / Binder / Lubricant / Protective Barrier (Engineered specifically utilizing High-Shear Wet Granulation to ensure 100% uniformity of the microscopic 1mg payload. The premium film coat protects the tablet from atmospheric moisture and masks the bitter taste of the tartrate salt). *Pack Sizes: 10×10 Blisters (Optimized specifically for 15-day to 30-day chronic GI dispensing regimens).
Cinnarizine & Dimenhydrinate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active antihistamine salts.
Active Ingredient Strength Primary Clinical Function Cinnarizine BP/USP 20 mg The Peripheral Stabilizer: Stops the influx of calcium into the inner ear hair cells to dampen the physical sensation of vertigo. Dimenhydrinate BP/USP 40 mg The Central Antiemetic: Blocks H1 and muscarinic receptors in the brain to prevent nausea and motion-induced vomiting. Excipients Microcrystalline Cellulose / Maize Starch / Talc / Magnesium Stearate / Croscarmellose Sodium Diluent / Binder / Glidant / Superdisintegrant (Engineered specifically utilizing High-Shear Dry Blending to ensure 100% uniformity of the active APIs, providing a rapid disintegration profile that delivers relief within 30 minutes of ingestion). *Pack Sizes: 10×10 Blisters (Optimized specifically for short-course acute vertigo regimens).
Cinnarizine Tablets
FreeTechnical & Manufacturing Specifications
Formulated for consistent release kinetics and long-term chemical stability.
Technical Metric Specification Standard Active Ingredient Cinnarizine BP / USP / IP Dosage Form Immediate Release Tablets Available Strengths 25 mg (Vestibular) / 75 mg (Cerebrovascular) HS Code 3004.90.39 (Other CNS drugs) / 2933.59.90 Stability Validated for Zone IVb (Tropical) export markets Ciprofloxacin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is non-negotiable due to the extreme bitterness of the API and its light sensitivity.
Active Ingredient Strength (Standard) Primary Role Ciprofloxacin HCl USP/BP 250 mg Uncomplicated UTI / Mild Infection Ciprofloxacin HCl USP/BP 500 mg Typhoid / Respiratory / Abdominal Ciprofloxacin HCl USP/BP 750 mg Severe / Bone & Joint / Pseudomonas Excipients Q.S. Titanium Dioxide (Opacifier) / Hypromellose Cisplatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution (Liquid) in amber glass vials.
Active Ingredient Strength Concentration Cisplatin USP/BP 10 mg Vial 1 mg/ml (10ml Vol) Cisplatin USP/BP 50 mg Vial 1 mg/ml (50ml Vol) Excipients Sodium Chloride / Mannitol Isotonicity / Diuresis *Pack Sizes: Tray of 1 Vial. (Cytotoxic Packaging).
Citalopram Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Bioavailability Tablet, packed exclusively in secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the chemical stability of the hydrobromide salt.
Active Ingredient Strength Primary Clinical Function Citalopram Hydrobromide USP/Ph.Eur. 10 mg / 20 mg The Primary Care Anchor: The definitive starting and maintenance doses utilized for the vast majority of patients with moderate depression or panic disorder. Citalopram Hydrobromide USP/Ph.Eur. 40 mg The Severe Refractory Payload: The maximum therapeutic dose utilized for severe depression. (Note: Doses above 40mg are strictly avoided due to cardiac risks). Excipients Lactose Monohydrate / Maize Starch / Croscarmellose Sodium / Magnesium Stearate / Hypromellose / Titanium Dioxide (Film Coat) Diluent / Binder / Superdisintegrant / Lubricant / Opaque Coating (Engineered specifically utilizing High-Shear Wet Granulation to ensure 100% uniformity of the active API, providing a smooth, fast-acting dissolution profile that matches the originator brand). *Pack Sizes: 10×10 Blisters or 28-Tablet Calendar Packs (Optimized for monthly psychiatric compliance).
Citicoline Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Citicoline Sodium USP/BP 500 mg 2 ml Ampoule (250 mg/ml) Citicoline Sodium USP/BP 1000 mg (1 g) 4 ml Ampoule (250 mg/ml) Excipients Water for Injection / pH Adjusters Preservative Free (Single Use) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Citicoline Sodium injection
FreeComposition
CT 1000 MG/4 ML INJECTION(AMPL)
Each ml contains- Citicoline Sodium IP
eq. to Citicoline 250mg + water for injection IP Q.S.
CT 500 MG/2ML INJECTION (AMPL)
Each ml contains- Citicoline Sodium IP
eq. to Citicoline 250mg + water for injection IP Q.S.
Usage: – used as a dietary supplement to support cognitive function
Category: – Citicoline Sodium injection
Therapeutic category: – Citicoline Sodium injection
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
Citicoline Tablets
FreeProduct Composition & Strength
We supply this product as Controlled Release (CR) Tablets (Film Coated). The matrix formulation is critical to extend the biological half-life.
Active Ingredient Strength Release Profile Primary Indication Citicoline Sodium USP/IP 500 mg Controlled Release Mild Cognitive Impairment / Maintenance Citicoline Sodium USP/IP 1000 mg Controlled Release Acute Stroke Recovery / Severe Dementia Excipients Q.S. HPMC (Release Retardant) / Magnesium Stearate Matrix System Clarithromycin Tablets
FreeClarithromycin Tablets USP 500 mg
Each Filmcoated tablet contains :
Clarithromycin USP 500 mgUsage: – Chest infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Clindamycin & clotrimazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Non-Greasy Vaginal Tablet (V-Tab), packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips, often accompanied by a specialized applicator for sterile insertion.
Active Ingredient Strength Primary Clinical Function Clindamycin Phosphate USP/Ph.Eur. 100 mg The Antibacterial Anchor: The definitive therapeutic unit utilized to eradicate anaerobic bacteria and restore the natural vaginal flora (Lactobacilli). Clotrimazole USP/Ph.Eur. 200 mg The Antifungal Payload: The massive imidazole payload required to penetrate deep into the mucosal layers and destroy recurrent yeast colonies. Excipients Adipic Acid / Sodium Bicarbonate / Lactose / Maize Starch / Magnesium Stearate Effervescent Matrix / Diluent / Disintegrant / Lubricant (Engineered specifically utilizing an Effervescent Vaginal Base. Upon contact with minimal vaginal moisture, the tablet releases microscopic amounts of CO2 to rapidly disperse the active APIs across the entire vaginal vault, ensuring no “untreated zones” remain) *Pack Sizes: 3-Tablet or 7-Tablet Strips (Optimized specifically for the strict, short-course clinical curative regimens).
Clindamycin Capsules
FreeClindamycin capsules are lincosamide antibiotics primarily used to treat serious bacterial infections, including those of the skin, lungs, and internal organs. They are most commonly formulated as Clindamycin Hydrochloride.
Clindamycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Clindamycin Phosphate USP/BP 300 mg 2 ml Ampoule (150 mg/ml) Clindamycin Phosphate USP/BP 600 mg 4 ml Ampoule (150 mg/ml) Excipients Benzyl Alcohol / EDTA Preservative / Stabilizer *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Clindipine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Light-Shielded Cardiovascular Tablet, packed exclusively in highly secure, opaque Alu-Alu blister strips to ensure the absolute chemical stability of the highly photosensitive active ingredient.
Active Ingredient Strength Primary Clinical Function Cilnidipine USP/Ph.Eur. 5 mg The Geriatric & Titration Anchor: The definitive starting dose utilized for elderly patients or those with mild essential hypertension to prevent sudden hypotensive episodes. Cilnidipine USP/Ph.Eur. 10 mg The Global Maintenance Standard: The standardized daily therapeutic payload utilized for the vast majority of adult patients requiring chronic 24-hour blood pressure control. Cilnidipine USP/Ph.Eur. 20 mg The Severe Refractory Macrodose: Utilized strictly for severe, uncontrolled hypertension where the 10mg dose has failed to achieve target blood pressure metrics. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Hypromellose / Magnesium Stearate / Opaque Polymeric Film (Titanium Dioxide base) Diluent / Densifier / Superdisintegrant / Binder / Lubricant / Protective Light Shield (Engineered specifically utilizing a dense, titanium dioxide-heavy film coat. Cilnidipine is intensely sensitive to UV and visible light; this opaque coating guarantees 100% of the active molecule survives to reach the patient’s systemic circulation) *Pack Sizes: 10×10 Opaque Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Clobazam Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The score line is critical for precise titration, especially in pediatric patients.
Active Ingredient Strength (Standard) Primary Role Clobazam USP/BP 5 mg Pediatric Initiation / Titration Clobazam USP/BP 10 mg Standard Maintenance Clobazam USP/BP 20 mg High Dose / Adult Refractory Excipients Q.S. Lactose / Maize Starch / Talc Clofazimine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Micronized Lipid-Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive phenazine dye.
Active Ingredient Strength Primary Clinical Function Clofazimine USP/Ph.Eur. 50 mg The Standard MDT Maintenance Unit: The globally standardized daily dose utilized in the WHO Multi-Drug Therapy (MDT) regimen for Multibacillary Leprosy. Clofazimine USP/Ph.Eur. 100 mg The MDR-TB & Acute ENL Macrodose: The heavy therapeutic payload utilized for the aggressive suppression of acute ENL reactions or as a core component of the standardized short-course MDR-TB regimen. Excipients Microcrystalline Cellulose / Propylene Glycol / Gelatin / Sodium Lauryl Sulfate / Magnesium Stearate / Heavy Opaque Polymeric Film Diluent / Lipid-Solvent Matrix / Binder / Surfactant / Lubricant / Protective Light Shield (Engineered specifically utilizing Advanced API Micronization & Solid-Lipid Tableting. Because Clofazimine is practically insoluble in water, the API is micro-milled and suspended in a specialized surfactant matrix to ensure it absorbs perfectly in the gut without requiring a soft-gelatin encapsulation process) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, continuous, multi-year infectious disease dispensing regimens).
Clomifene citrate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Light-Shielded Fertility Tablet, packed exclusively in highly secure, opaque Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the photosensitive SERM.
Active Ingredient Strength Primary Clinical Function Clomifene Citrate USP/Ph.Eur. 50 mg The Standard Ovulatory Anchor: The definitive starting dose utilized for the first cycle of ovulation induction to assess ovarian response and minimize the risk of dangerous hyperstimulation. Clomifene Citrate USP/Ph.Eur. 100 mg The Refractory Macrodose: The heavy therapeutic payload utilized strictly for subsequent cycles in patients who failed to ovulate (clomifene-resistant PCOS) on the 50mg dose. Excipients Lactose Monohydrate / Maize Starch / Pregelatinized Starch / Magnesium Stearate / Opaque Polymeric Film (Titanium Dioxide base) Diluent / Binder / Disintegrant / Lubricant / Protective Light Shield (Engineered specifically utilizing a dense, titanium dioxide-heavy film coat. Clomifene degrades under direct UV/visible light; this opaque coating guarantees 100% of the active hormone modulator survives from the blister pack to the patient’s stomach) *Pack Sizes: 10-Tablet or 5-Tablet Blisters (Optimized specifically for the strict, 5-day cyclical dosing regimen utilized in reproductive endocrinology).
Clonazepam Tablets
FreeProduct Composition & Available Strengths
We supply Clonazepam across the complete, internationally standardized therapeutic spectrum to facilitate precise titration for both pediatric epilepsy and high-potency adult neurological control.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Clonazepam USP / BP / IP 0.5 mg
(500 mcg)
Oral / Sublingual Micro-Tablet Epilepsy Titration / Panic Baseline: For pediatric seizure disorders, low-dose stabilization, and initial panic management. Clonazepam USP / BP / IP 1.0 mg
(1000 mcg)
Oral / Sublingual Micro-Tablet Intermediate Maintenance: Step-up strength optimized for routine daily neurological maintenance without expanding tablet counts. Clonazepam USP / BP / IP 2.0 mg
(2000 mcg)
Oral High-Potency Solid Tablet Refractory Epilepsy & Acute Care: High-strength configuration calibrated for status epilepticus prophylaxis, myoclonic spasms, and manic stabilization. Clonidine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Small, White). Note: Clonidine is extremely potent and dosed in micrograms (mcg), not milligrams.
Active Ingredient Strength (Metric) Strength (Common) Primary Role Clonidine HCl USP/BP/IP 100 mcg 0.1 mg Initiation / Mild Hypertension Clonidine HCl USP/BP/IP 200 mcg 0.2 mg Standard Maintenance Clonidine HCl USP/BP/IP 300 mcg 0.3 mg High Dose / Crisis Management Excipients Q.S. Lactose / Corn Starch Filler / Binder Clopidogrel & Aspirin Capsules
FreeClopidogrel and Aspirin capsules are a combination of two antiplatelet medications (blood thinners) used primarily to prevent heart attacks and strokes in patients with high cardiovascular risk.
Clopidogrel, Aspirin Tablets Clopidogrel, Aspirin Tablets
FreeA Clopidogrel + Aspirin tablet is a dual antiplatelet therapy (DAPT) used primarily to prevent serious cardiovascular events like heart attacks and strokes
Clotrimazole Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Vaginal Tablets (bullet or almond shaped) with or without an applicator, offering flexible treatment durations.
Active Ingredient Strength Treatment Course Patient Convenience Clotrimazole USP/BP 100 mg 6 Nights Standard Therapy Clotrimazole USP/BP 200 mg 3 Nights Short Course Clotrimazole USP/BP 500 mg 1 Night Single Dose (“One Shot”) Excipients Q.S. Lactose / Adipic Acid / Starch Rapid Disintegration Cloxacillin Capsules
FreeCloxacillin capsules are penicillin-type antibiotics used specifically to treat infections caused by staphylococci (staph infections) that produce an enzyme called penicillinase.
Cloxacillin 1gm Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cloxacillin Sodium USP/BP Equivalent to 1000 mg (1 g) Cloxacillin Severe Infection / Surgery Sodium Content Approx 2.3 mEq (53 mg) per gram Monitor in Heart Failure *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Cloxacillin 500mg Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cloxacillin Sodium USP/BP Equivalent to 500 mg Cloxacillin Adult Standard Dose Cloxacillin Sodium USP/BP Equivalent to 250 mg Pediatric Dose Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, 50 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
Clozapine Tablets
FreeProduct Composition & Available Titration Strengths
Because Clozapine demands highly delicate, low-dose initial titration to protect the patient’s cardiovascular profile, we manufacture the full compendial strength spectrum.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Clozapine USP / BP / IP 25 mg Oral Solid Uncoated Micro-Tablet Introductory Safety Titration: Mandatory low-dose baseline format utilized exclusively for the initial day 1 and day 2 dose-escalation phase to prevent orthostatic shock. Clozapine USP / BP / IP 50 mg Oral Solid Uncoated Micro-Tablet Intermediate Dose Step-Up: Mid-tier titration strength engineered to scale up systemic tolerance during weeks 1 and 2. Clozapine USP / BP / IP 100 mg Oral Solid Compressed Tablet The Core Commercial Volume: First-line international standard target maintenance strength for adult refractory schizophrenia management. Co -Trimoxazole Tablets Tablet
FreeCo- Trimoxazole Tablets IP
Trimethoprime & Sulphamethoxazole Tablets IP
Each Uncoated tablet contains :
Trimethoprime IP 20 mg
Sulphamethoxazole IP 100 mgTrimethoprim & sulphamethoxazole tablets IP Co -trimoxazole Tablets IP
Each film coated tablets : Excipients q.s
Trimethoprim IP 80 mg
Sulphamethoxazole IP 400 mgTrimethoprim & sulphamethoxazole tablets IP
Each film coated tablets :
Trimethoprim IP 160 mg
Sulphamethoxazole IP 800 mgCo – Trimoxazole Tablets BP
Trimethoprim & Sulphamethoxazole Tablets BP
Each Uncoated Tablet contains :
Trimethoprim BP 80 mg
Sulfamethoxazole BP 400 mgTACOT – DS
Trimethoprim & Sulphamethoxazole Tablets BP
Each Uncoated tablet contains :
Trimethoprim BP 160 mg
Sulphamethoxazole BP 800 mgUsage: – Traveler’s diarrhea
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Codeine Phosphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Narcotic Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the alkaloid salt and to strictly prevent diversion.
Active Ingredient Strength Primary Clinical Function Codeine Phosphate USP/Ph.Eur. 15 mg / 30 mg The Standard Analgesic / Antitussive Anchor: The definitive unit utilized for the suppression of severe, dry coughs and the management of mild-to-moderate acute somatic pain. Codeine Phosphate USP/Ph.Eur. 60 mg The Severe Trauma Macrodose: The heavy therapeutic payload utilized strictly for moderate-to-severe refractory pain, often in post-operative or palliative oncology settings. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Densifier / Superdisintegrant / Lubricant / Glidant (Engineered utilizing Strict Geometric Dilution to ensure the opiate payload is flawlessly uniform across every batch, preventing toxic “hot spots” that could trigger accidental respiratory depression) *Pack Sizes: 10×10 Tamper-Evident Blisters (Optimized specifically for strict, closely monitored acute pain dispensing regimens).
Colistimethate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials. Strength is measured in International Units (IU).
Strength (IU) Approximate Mass (mg) Colistin Base Activity (CBA) 1 MIU (1 Million IU) ~80 mg CMS ~34 mg CBA 2 MIU ~160 mg CMS ~68 mg CBA 3 MIU ~240 mg CMS ~100 mg CBA 4.5 MIU ~360 mg CMS ~150 mg CBA Excipients None (Pure Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Collagen Peptide , Sodium Hyaluronate , Chondroitin Sulfate and Vitamin C Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical survival of the intensely sensitive biological payloads.
Active Ingredient Strength Primary Clinical Function Hydrolyzed Collagen Peptides (Type I & II) 150 mg – 500 mg
(Customizable per monograph)The Structural Foundation: The massive, highly bioavailable amino acid payload required to stimulate chondrocyte proliferation and rebuild the physical cartilage matrix. Chondroitin Sulfate Sodium USP/Ph.Eur. 200 mg The Cartilage Hydrator & Shield: Prevents enzymatic cartilage degradation and draws essential water into the articular matrix for compression resistance. Sodium Hyaluronate (Hyaluronic Acid) 30 mg The Synovial Lubricant: Restores the high-viscosity, shock-absorbing properties of the joint capsule fluid. Vitamin C (Ascorbic Acid) USP/Ph.Eur. 35 mg The Biosynthetic Cofactor: The absolute mandatory catalyst required to cross-link the newly formed collagen fibers into a strong, unified matrix. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Glidant / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced Cold-Process High-Shear Granulation. Fluffy collagen peptides are heavily densified without using destructive heat that would instantly oxidize and destroy the Vitamin C payload) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30/60 (Optimized specifically for premium retail presentation and chronic daily compliance).
Corion
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials with a specific solvent.
Active Ingredient Strength (IU) Primary Use Chorionic Gonadotropin USP/BP 5000 IU Standard Ovulation Trigger Chorionic Gonadotropin USP/BP 10000 IU High Dose / IVF Trigger Chorionic Gonadotropin USP/BP 2000 IU Male Hypogonadism / Maintenance Solvent Sodium Chloride (Isotonic) 1 ml or 2 ml Ampoule *Pack Sizes: Tray of 1 Vial + Solvent, 5 Vials + Solvents.
Cyanocobalamin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Standard Use Cyanocobalamin USP/BP 1000 mcg (1 mg) / ml Adult Therapeutic Dose Cyanocobalamin USP/BP 500 mcg / ml Maintenance / Pediatric Excipients Sodium Chloride / Benzyl Alcohol Isotonicity / Preservative *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Cyclophosphamide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Cyclophosphamide USP/BP 200 mg Vial Low Dose / Autoimmune Cyclophosphamide USP/BP 500 mg Vial Standard Chemotherapy Cyclophosphamide USP/BP 1000 mg (1 g) Vial High Dose / Hematology Excipients Mannitol / Sodium Chloride Bulking Agent (For Cake Structure) *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Cyclophosphamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Cytotoxic Prodrug Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the sensitive nitrogen mustard derivative and to physically protect caregivers from API exposure.
Active Ingredient Strength Primary Clinical Function Cyclophosphamide USP/Ph.Eur.
(as Cyclophosphamide Monohydrate)50 mg The Oncology & Autoimmune Macrodose: The definitive oral therapeutic unit utilized for chronic, daily continuous “metronomic” chemotherapy regimens and severe immunosuppressive maintenance. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Starch / Magnesium Stearate / Heavy Sucrose or Polymeric Film-Coat Diluent / Densifier / Disintegrant / Lubricant / Protective Cytotoxic Shield (Engineered specifically utilizing a thick, impenetrable sugar or film coat to ensure the highly toxic API never comes into contact with the skin of the patient, pharmacist, or caregiver handling the pill) *Pack Sizes: Bottles of 50/100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic oncology and rheumatology dispensing regimens).
Cyclosporine tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, SMEDDS Liquid-Filled Soft Gelatin Capsule, packed exclusively in highly secure, moisture-resistant heavy-gauge Alu-Alu blister strips to ensure the absolute chemical and physical stability of the volatile microemulsion.
Active Ingredient Strength Primary Clinical Function Cyclosporine USP/Ph.Eur. (Modified) 25 mg / 50 mg The Micro-Titration Anchor: The definitive units utilized for extremely precise, weight-based dose adjustments during the critical early post-transplant phase, or for pediatric dosing. Cyclosporine USP/Ph.Eur. (Modified) 100 mg The Transplant Macrodose: The heavy therapeutic payload required to minimize the total pill burden for adult patients maintaining long-term solid organ graft survival. Excipients (SMEDDS Matrix) Polyoxyl 40 Hydrogenated Castor Oil / Polysorbate 80 / Propylene Glycol / Corn Oil Mono-di-triglycerides / Alpha-Tocopherol Microemulsion Vehicles & Surfactants / Co-Solvent / Lipophilic Carrier / Antioxidant (Engineered specifically to keep the massive lipophilic peptide fully dissolved inside the gelatin shell, instantly forming nanometer-sized droplets upon contact with stomach acid for maximum bioavailability) *Pack Sizes: 5×10 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, lifelong immunosuppressive dispensing regimens).
Cytarabine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution (Liquid) or Lyophilized Powder.
Active Ingredient Strength Format Cytarabine USP/BP 100 mg / 5 ml (20 mg/ml) Ready-to-use Liquid Cytarabine USP/BP 500 mg / 10 ml (50 mg/ml) Ready-to-use Liquid Cytarabine USP/BP 1000 mg (1 g) Vial Lyophilized Powder or Conc. Liquid Excipients Water for Injection Preservative-Free (Available for IT use) *Pack Sizes: Tray of 1 Vial, 5 Vials, or Box of 1/10 Vials.
Dabigatran Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Tartaric Acid-Cored Pellet Formulation, packed exclusively in highly specialized, moisture-blocking Alu-Alu blister strips with integrated desiccants to ensure the absolute chemical survival of the intensely hygroscopic prodrug.
Active Ingredient Strength Primary Clinical Function Dabigatran Etexilate Mesylate USP/Ph.Eur. 75 mg / 110 mg The Renal & Geriatric Anchor: The strictly mandated dose reductions utilized for elderly patients (over 80 years old), patients with moderate renal impairment, or those at an elevated risk of hemorrhagic bleeding. Dabigatran Etexilate Mesylate USP/Ph.Eur. 150 mg The Cardiovascular Macrodose: The massive, globally standardized therapeutic payload required for the aggressive, daily prevention of stroke and systemic embolism in Non-Valvular Atrial Fibrillation (NVAF). Excipients Tartaric Acid (Core) / Hypromellose / Talc / Hydroxypropyl Cellulose / Dimethicone Acidic Microenvironment Generator / Polymer Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced Fluid-Bed Pellet Coating. The tartaric acid core is isolated with a polymer layer, then coated with the Dabigatran API, and sealed again. This prevents the acid from prematurely degrading the drug before it reaches the patient’s stomach) *Pack Sizes: 10×10 Specialized Alu-Alu Blisters or Heavy-Gauge HDPE Bottles with Desiccant Caps (Optimized specifically for absolute moisture defense).
Dacarbazine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in amber glass vials to protect from light.
Active Ingredient Strength Therapeutic Role Dacarbazine USP/BP (DTIC) 200 mg Vial Standard Dose Dacarbazine USP/BP (DTIC) 500 mg Vial High Dose / Multi-use Excipients Citric Acid, Mannitol Stabilizers / pH Adjusters *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Daclatasvir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dihydrochloride Salt Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the active virological agent.
Active Ingredient Strength Primary Clinical Function Daclatasvir Dihydrochloride USP/Ph.Eur. 60 mg The Standard Eradication Macrodose: The definitive, globally standardized daily therapeutic payload utilized for the vast majority of patients to achieve a Sustained Virologic Response (SVR12 – Clinical Cure). Daclatasvir Dihydrochloride USP/Ph.Eur. 30 mg The CYP3A4 Titration Unit: The strict, mandatory dose-reduction unit utilized for patients who are co-infected with HIV and taking strong CYP3A inhibitors (like Ritonavir or Atazanavir). Excipients Anhydrous Lactose / Microcrystalline Cellulose / Croscarmellose Sodium / Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film (Opadry Green) Diluent / Densifier / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced dissolution-enhancing matrices to ensure the Dihydrochloride salt separates perfectly in gastric fluid, guaranteeing maximum systemic bioavailability) *Pack Sizes: Heavy-Gauge HDPE Bottles of 28 (Optimized exactly for a 4-week supply in strict 12-week or 24-week curative regimens).
Dapagliflozin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive propanediol monohydrate active ingredient.
Active Ingredient Strength Primary Clinical Function Dapagliflozin (as Propanediol Monohydrate) USP/Ph.Eur. 5 mg The Titration & Hepatic Anchor: The definitive starting dose utilized for patients with severe hepatic impairment or those at high risk for volume depletion (hypotension). Dapagliflozin (as Propanediol Monohydrate) USP/Ph.Eur. 10 mg The Cardio-Renal Macrodose: The massive, globally standardized therapeutic payload required for the aggressive, daily maintenance of Heart Failure, CKD, and Type 2 Diabetes. Excipients Microcrystalline Cellulose / Anhydrous Lactose / Crospovidone / Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Densifier / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing Strict Low-Humidity Granulation to prevent the highly sensitive API from degrading during compression, sealed with an impenetrable film-coat to block environmental moisture and ensure rapid gastric dissolution) *Pack Sizes: 10×10 Alu-Alu Blisters or 14/28-Tablet Calendar Packs (Optimized specifically for strict chronic cardio-renal dispensing regimens).
Dapsone Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White). The range of strengths allows for precise dosing in both leprosy programs and dermatological maintenance.
Active Ingredient Strength (Standard) Primary Role Dapsone USP/BP 25 mg Pediatric / Initiation Dapsone USP/BP 50 mg Intermediate Dose Dapsone USP/BP 100 mg Standard Adult MDT Dose Excipients Q.S. Magnesium Stearate / Starch Darifenacin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix Prolonged-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute physical stability of the controlled-release polymer.
Active Ingredient Strength Primary Clinical Function Darifenacin Hydrobromide USP/Ph.Eur.
(Equivalent to Darifenacin base)7.5 mg (PR) The Standard Titration & Geriatric Anchor: The definitive, highly efficacious starting and maintenance dose utilized for the vast majority of patients to control OAB symptoms with minimal side effects. Darifenacin Hydrobromide USP/Ph.Eur. 15 mg (PR) The Severe Refractory Macrodose: High-efficacy therapeutic payload utilized strictly for patients who require greater symptom relief and have demonstrated high tolerability to the 7.5 mg dose. Excipients Hypromellose (HPMC) / Dibasic Calcium Phosphate / Magnesium Stearate / Polyethylene Glycol / Titanium Dioxide / Premium Polymeric Film Hydrophilic PR Matrix / Diluent / Lubricant / Plasticizer / Opaque Film (Engineered specifically utilizing high-viscosity Hypromellose. Upon contact with gastrointestinal fluids, the tablet hydrates to form a thick, gelatinous outer layer that strictly controls the diffusion of the highly soluble hydrobromide salt over a 24-hour period) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic urological dispensing regimens).
Daunorubicin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in red-capped glass vials.
Active Ingredient Strength Appearance Daunorubicin Hydrochloride USP/BP Equivalent to 20 mg Daunorubicin Red-Orange Lyophilized Cake Excipients Mannitol Bulking Agent *Pack Sizes: Tray of 1 Vial. (Cytotoxic Packaging).
Deferasirox Tablets
FreeProduct Composition & Strength
We supply this product across two distinct, Precision-Blended Engineering Platforms, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute physical and chemical stability of the active pharmaceutical ingredient.
Active Ingredient Strength & Form Primary Clinical Function Deferasirox USP/Ph.Eur. 125 mg / 250 mg / 500 mg (Dispersible) The Pediatric Suspension Standard: Engineered with micro-crystalline disintegrants to rapidly dissolve in water or apple juice for precise, weight-based pediatric dosing. Deferasirox USP/Ph.Eur. 90 mg / 360 mg (Film-Coated) The High-Compliance Macrodose: The highly densified, lactose-free therapeutic payload designed to be swallowed whole, minimizing GI distress for adult patients. (Note: 360mg FCT is clinically equivalent to 500mg DT). Excipients (FCT Matrix) Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Poloxamer 188 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Solubilizer / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced High-Shear Wet Granulation and Poloxamer Solubilization. Because the FCT tablet is highly densified, it requires elite surfactants to guarantee instantaneous release and absorption in the gastrointestinal tract without the need for pre-dispersion) *Pack Sizes: 10×10 Alu-Alu Blisters or Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for strict, 30-day chronic hematology dispensing regimens).
Deferiprone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, heavy-gauge HDPE bottles to ensure the absolute physical and chemical stability of the massive active pharmaceutical payload.
Active Ingredient Strength Primary Clinical Function Deferiprone USP/Ph.Eur. 500 mg The Standard Titration Unit: The baseline therapeutic dose utilized for precise, weight-based titration in pediatric and lower-weight thalassemia patients. Deferiprone USP/Ph.Eur. 1000 mg The Hematology Macrodose: The massive therapeutic payload required to minimize the total daily pill burden for adult patients suffering from severe, refractory iron overload. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced High-Shear Wet Granulation. Because a 1000mg tablet is inherently massive, it must be highly densified to remain swallowable, heavily coated to mask its severe bitterness, and packed with elite disintegrants to ensure it shatters instantly in the stomach) *Pack Sizes: Heavy-Gauge HDPE Bottles of 50 or 100 (Optimized specifically for massive, multi-pill daily chronic dispensing regimens).
Deflazacort Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Steroidal Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the glucocorticoid prodrug.
Active Ingredient Strength Primary Clinical Function Deflazacort USP/Ph.Eur. 6 mg The Pediatric & Titration Standard: The definitive unit utilized for weight-based dosing in pediatric Duchenne Muscular Dystrophy, slow tapering protocols, and chronic low-dose maintenance for rheumatoid arthritis. Deflazacort USP/Ph.Eur. 30 mg The Acute Flare-Up Macrodose: High-efficacy therapeutic payload utilized for the immediate, aggressive suppression of severe allergic anaphylaxis, acute asthma exacerbations, and violent autoimmune flare-ups. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Binder / Superdisintegrant / Lubricant / Glidant (Engineered utilizing Extreme Multi-Stage Geometric Dilution to ensure the steroidal payload is flawlessly uniform, manufactured under strict OEB 4 containment protocols to prevent cross-contamination and protect facility operators) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict titration, tapering, and chronic immunological dispensing regimens).
Desloratidine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Dissolution Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent API.
Active Ingredient Strength Primary Clinical Function Desloratadine USP/Ph.Eur. 5 mg The Global Allergy & Dermatology Anchor: The definitive once-daily therapeutic unit utilized for the continuous, 24-hour baseline control of Allergic Rhinitis (Hay Fever) and severe Chronic Urticaria. Excipients Microcrystalline Cellulose / Dibasic Calcium Phosphate / Maize Starch / Talc / Premium Polymeric Film Diluent / Densifier / Disintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing elite rapid-burst disintegrants to ensure the tablet shatters instantly in gastric fluid. The dense polymer coating masks the inherent bitterness of the API, ensuring a flawless patient experience) *Pack Sizes: 10×10 Blisters or Bottles of 30 (Optimized specifically for strict, 30-day chronic allergy and dermatology dispensing regimens).
Desmopressin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extreme Microdose Peptide Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical stability of the fragile acetate salt.
Active Ingredient Strength Primary Clinical Function Desmopressin Acetate USP/Ph.Eur.
(Equivalent to Desmopressin base)0.1 mg The Titration & Pediatric Anchor: The definitive starting dose utilized for primary nocturnal enuresis in children or baseline control of Central Diabetes Insipidus. Desmopressin Acetate USP/Ph.Eur. 0.2 mg The Maintenance Macrodose: High-efficacy therapeutic payload utilized for severe, refractory polyuria and nocturia in adults. Excipients Lactose Monohydrate / Potato Starch / Povidone K-30 / Magnesium Stearate Diluent / Disintegrant / Binder / Lubricant (Engineered specifically utilizing Strict Geometric Dilution to ensure the microscopic peptide payload is flawlessly uniform, manufactured under stringent low-moisture conditions to prevent hydrolytic degradation of the fragile peptide bonds) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30/100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic endocrine dispensing regimens).
Desvenlafaxine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix Extended-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical and physical stability of the controlled-release polymer.
Active Ingredient Strength Primary Clinical Function Desvenlafaxine Succinate USP/Ph.Eur.
(Equivalent to Desvenlafaxine base)50 mg (ER) The Global Therapeutic Standard: The definitive, highly efficacious starting and maintenance dose utilized for the vast majority of patients suffering from Major Depressive Disorder. Desvenlafaxine Succinate USP/Ph.Eur. 100 mg (ER) The Severe Refractory Macrodose: High-efficacy therapeutic payload utilized strictly for severe, treatment-resistant depression where maximum norepinephrine reuptake inhibition is required. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Talc / Magnesium Stearate / Premium Polymeric Film Hydrophilic ER Matrix / Diluent / Glidant / Lubricant / Film-Coating (Engineered specifically utilizing high-viscosity Hypromellose. Upon contact with gastric fluid, the tablet forms a thick, gelatinous outer layer that slowly erodes over 24 hours, guaranteeing a smooth, flat pharmacokinetic curve to prevent violent nausea and serotonin spikes) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day psychiatric dispensing regimens).
Dexamethasone injection
FreeComposition
Dexamethasone 4mg/ 20 ml Vial
Dexamethasone 4mg/ 2 ml Vial
Pcd pharma franchise:-
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Dexamethasone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Dexamethasone Sodium Phosphate USP/BP 4 mg (Standard) 1 ml Ampoule (4 mg/ml) Dexamethasone Sodium Phosphate USP/BP 8 mg (High Dose) 2 ml Ampoule (4 mg/ml) Dexamethasone Sodium Phosphate USP/BP 20 mg (Multi-Dose) 5 ml Vial (4 mg/ml) Excipients Creatinine / Sodium Citrate Stabilizers / Buffers *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Dexamethasone Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (typically White, Round, Scored). The scoring allows for precise dose tapering.
Active Ingredient Strength (Standard) Therapeutic Role Dexamethasone USP/BP 0.5 mg Standard Low Dose / Pediatric Dexamethasone USP/BP 4 mg High Dose / Pulse Therapy Dexamethasone USP/BP 8 mg Critical Care / Oncology Excipients Q.S. Lactose / Corn Starch / Magnesium Stearate Diluent / Lubricant Dexlansoprazole & Domperidone Capsules
FreeDexlansoprazole and Domperidone capsules are a combination medication primarily used for erosive esophagitis and Gastroesophageal Reflux Disease (GERD). This combination reduces stomach acid while also speeding up gastric emptying to prevent reflux.
Dexrabeprazole Sodium & Cinitapride Capsules
FreeDexrabeprazole Sodium and Cinitapride capsules are a combination therapy used to treat gastrointestinal disorders such as GERD, peptic ulcers, and delayed gastric emptying. This combination addresses both acid production and gut motility issues.
Dexrabeprazole Sodium & Domperidone Capsules
FreeDexrabeprazole Sodium and Domperidone capsules are combination medications used to treat acid reflux, GERD, and peptic ulcers. They combine a potent acid reducer with a medicine that speeds up stomach emptying.
DI Calcium Phosphate with Vitamin D3 Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (typically White, Round/Oval). The formulation is optimized for disintegration to prevent the “gritty” sensation often associated with phosphate salts.
Active Ingredient Strength (Standard) Therapeutic Role Dibasic Calcium Phosphate IP/USP 500 mg / 1000 mg Source of Calcium & Phosphorus Vitamin D3 (Cholecalciferol) IP/USP 200 IU / 400 IU Absorption Enhancer Excipients Q.S. Maize Starch / Gelatin / Talc Binder / Glidant Diacerein & Glucosamine Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the intensely hygroscopic Glucosamine salt.
Active Ingredient Strength Primary Clinical Function Diacerein USP/Ph.Eur. 50 mg The IL-1β Inhibitor: The potent, slow-acting anti-inflammatory anchor required to halt the enzymatic digestion of joint cartilage. Glucosamine Sulphate Potassium Chloride USP/Ph.Eur.
(Equivalent to Glucosamine Sulphate 750mg)750 mg The Cartilage Substrate: The massive amino-sugar payload required to stimulate proteoglycan synthesis and rebuild the articular matrix. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced Low-Humidity Granulation Technology to process the sticky, highly hygroscopic Glucosamine, sealed with a dense polymer film to block environmental moisture and ensure rapid gastric dissolution of the highly insoluble Diacerein) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, continuous, long-term chronic dispensing regimens).
Diacerein Capsules
FreeDiacerein capsules are a slow-acting treatment primarily used for osteoarthritis of the knee and hip. They work by inhibiting Interleukin-1 (IL-1), a protein that plays a major role in joint inflammation and the destruction of cartilage.
Diazepam Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The score line allows for flexible dosing.
Active Ingredient Strength (Standard) Primary Indication Diazepam USP/BP 2 mg Geriatric / Mild Muscle Spasm Diazepam USP/BP 5 mg Standard Anxiety Dose Diazepam USP/BP 10 mg Severe Spasm / Alcohol Withdrawal Excipients Q.S. Lactose / Maize Starch Diclofenac Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. Sugar coating is traditional to effectively mask the bitter taste of the API.
Active Ingredient Strength (Standard) Primary Indication Diclofenac Potassium USP/BP 25 mg Pediatric (Older) / Mild Pain Diclofenac Potassium USP/BP 50 mg Standard Adult Acute Dose Diclofenac Potassium USP/BP 75 mg Severe Acute Pain (Post-Op) Excipients Q.S. Sucrose (Coating) / Maize Starch Diclofenac Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Reddish-Brown or White). The coating is essential to mask the intensely bitter and metallic taste of the potassium salt.
Active Ingredient Strength (Standard) Therapeutic Role Diclofenac Potassium USP/BP 25 mg Pediatric (Older Children) / Mild Pain Diclofenac Potassium USP/BP 50 mg Standard Acute Adult Dose Excipients Q.S. Maize Starch / Povidone / Sucrose Disintegrant / Coating Agent Diclofenac Sodium & Serratiopeptidase Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Multi-Particulate or Bilayer Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the sensitive biological enzyme.
Active Ingredient Strength Primary Clinical Function Diclofenac Sodium USP/Ph.Eur. 50 mg Potent peripheral NSAID for sustained localized pain and inflammation blockade. Serratiopeptidase IP/Ph.Eur. 10 mg or 15 mg (Enteric-Coated) Proteolytic enzyme engineered to drain localized post-surgical/traumatic edema. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Magnesium Stearate Enteric Coating Polymer for Serratiopeptidase / Diluent / Lubricant *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for 7-to-14 day post-operative or orthopedic recovery regimens).
Diclofenac Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. We offer both the standard 3ml volume and the advanced 1ml (AQ) technology.
Active Ingredient Strength Technology Variant Diclofenac Sodium USP/BP 75 mg / 3 ml Standard (Propylene Glycol Base) Diclofenac Sodium USP/BP 75 mg / 1 ml AQ / Dynapar Generic (Painless, Water Base) Excipients Benzyl Alcohol / Mannitol Preservative / Stabilizer *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Diclofenac Sodium Paracetamol Serratiopeptidase Tablets
FreeA tablet containing Diclofenac Sodium + Paracetamol + Serratiopeptidase is a triple-action medication formulated to provide comprehensive relief from pain, fever, and inflammation. It is widely used for musculoskeletal disorders, post-surgical recovery, and dental pain.
Diclofenac Tablets
FreeProduct Composition & Strength
We supply this product as Enteric Coated (Gastro-Resistant) Tablets or Sustained Release (SR) Tablets.
Active Ingredient Strength (Standard) Formulation Role Diclofenac Sodium USP/BP 25 mg Enteric Coated Pediatric / Mild Pain Diclofenac Sodium USP/BP 50 mg Enteric Coated Standard Acute Dose Diclofenac Sodium USP/BP 75 mg Enteric Coated / SR Intermediate / Injection Switch Diclofenac Sodium USP/BP 100 mg Sustained Release (SR) Once Daily (Chronic Pain) Dicyclomine & Mefenic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Dicyclomine Hydrochloride USP/Ph.Eur. 10 mg The Anticholinergic Anchor: The potent antimuscarinic payload required to rapidly force smooth muscle relaxation and dry up hyper-secretions in the gut. Mefenamic Acid USP/Ph.Eur. 250 mg The Gynecological Analgesic Payload: The dual-action fenamate NSAID required to crush radiating inflammatory pain and block uterine prostaglandin receptors. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Enteric-Like Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing Bi-Layer Compression Technology to physically separate the highly reactive Dicyclomine from the bulky Mefenamic Acid, ensuring rapid, synchronized gastric dissolution without the APIs degrading each other) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute gynecological and GI dispensing regimens).
Dicyclomine HCL Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Dicyclomine Hydrochloride USP/BP 20 mg 2 ml Ampoule (10 mg/ml) Excipients Sodium Chloride / Water for Injection Isotonic Vehicle *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Dicyclomine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (usually small, white or blue). The dosage allows for flexible titration based on the severity of spasms.
Active Ingredient Strength (Standard) Primary Role Dicyclomine HCl USP/BP/IP 10 mg Pediatric / Mild Cramps Dicyclomine HCl USP/BP/IP 20 mg Adult Standard / IBS Therapy Excipients Q.S. Lactose / Magnesium Stearate Didanosine Capsules
FreeDidanosine capsules, often known by the brand name Videx EC, are delayed-release antiretroviral medications used to treat HIV. They are specifically formulated as enteric-coated beadlets within a capsule to prevent the active medicine from being destroyed by stomach acid.
Dienogest Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent steroidal API.
Active Ingredient Strength Primary Clinical Function Dienogest USP/Ph.Eur. 2 mg The Global Endometriosis Standard: The definitive therapeutic micro-dose utilized globally for the continuous, long-term suppression of pelvic pain, dysmenorrhea, and dyspareunia caused by endometriosis. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the 2mg steroidal payload is flawlessly uniform, finished with an opaque film-coat to seal the potent hormone safely away from factory handlers) *Pack Sizes: 14/28-Tablet Calendar Blisters (Optimized specifically for daily, uninterrupted, long-term gynecological dispensing).
Diethyl Carbamazine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White, circular). The formulation is designed for rapid disintegration to support mass dosing campaigns.
Active Ingredient Strength (Standard) Primary Role Diethylcarbamazine Citrate USP/BP/IP 50 mg Pediatric / Titration Diethylcarbamazine Citrate USP/BP/IP 100 mg Standard Adult Unit Diethylcarbamazine Citrate USP/BP/IP 300 mg (Forte) High Dose / TPE Therapy Excipients Q.S. Dibasic Calcium Phosphate / Starch Digoxin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules.
Active Ingredient Strength Concentration Digoxin USP/BP 500 mcg (0.5 mg) 250 mcg/ml (2 ml Ampoule) Excipients Propylene Glycol / Alcohol Solubilizers (Critical for stability) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Digoxin Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). Due to the potency (measured in micrograms), precise titration options are essential.
Active Ingredient Strength (Standard) Target Patient Digoxin USP/BP/IP 0.0625 mg (62.5 mcg) Pediatric / Severe Renal Failure Digoxin USP/BP/IP 0.125 mg (125 mcg) Geriatric / Maintenance Digoxin USP/BP/IP 0.25 mg (250 mcg) Standard Adult Dose Excipients Q.S. Lactose / Maize Starch Diloxanide Furoate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Luminal-Dispersion Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the anti-parasitic ester.
Active Ingredient Strength Primary Clinical Function Diloxanide Furoate USP/Ph.Eur. 500 mg The Global Anti-Parasitic Standard: The definitive therapeutic macrodose utilized globally for the total luminal eradication of amoebic cysts in asymptomatic carriers and post-dysentery patients. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced high-shear granulation and elite superdisintegrants to ensure the massive 500mg tablet shatters and disperses uniformly across the intestinal lining, maximizing physical contact with the embedded cysts) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, 10-day acute parasitology eradication regimens).
Diltiazem Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Immediate Release) or Sustained Release (SR) Tablets (Matrix Technology).
Active Ingredient Strength Formulation Role Diltiazem HCl USP/BP 30 mg Immediate Release Initial Titration / Angina Diltiazem HCl USP/BP 60 mg Immediate Release Standard Maintenance Diltiazem HCl USP/BP 90 mg / 120 mg Sustained Release (SR) Twice Daily Control Excipients Q.S. HPMC (Release Matrix) / Lactose Controlled Diffusion Diphenoxylate & Atropine Sulfate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extreme Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of both the opioid and the anticholinergic alkaloid.
Active Ingredient Strength Primary Clinical Function Diphenoxylate Hydrochloride USP/Ph.Eur. 2.5 mg The Anti-Diarrheal Anchor: The potent mu-opioid agonist required to physically halt hyperactive intestinal peristalsis. Atropine Sulfate USP/Ph.Eur. 0.025 mg (25 mcg) The Abuse Deterrent (Ultra-Microdose): The anticholinergic alkaloid engineered strictly to prevent deliberate opioid overdosage. Excipients Microcrystalline Cellulose / Sucrose / Maize Starch / Magnesium Stearate / Purified Talc Diluent / Binder / Disintegrant / Lubricant / Glidant (Engineered utilizing Extreme Multi-Stage Geometric Dilution to guarantee the microscopic 25 microgram Atropine payload is flawlessly distributed throughout the tablet, preventing lethal anticholinergic “hot spots”) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute gastrointestinal dispensing regimens).
Diphenylhydantoin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dissolution-Optimized Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive sodium salt.
Active Ingredient Strength Primary Clinical Function Diphenylhydantoin (Phenytoin) Sodium USP/Ph.Eur. 100 mg The Global Epilepsy Standard: The definitive therapeutic unit utilized globally for the chronic, daily maintenance and suppression of tonic-clonic and psychomotor seizures. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Povidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant / Lubricant (Engineered specifically utilizing Strict Particle-Size Distribution (PSD) Control. Because the drug is highly insoluble, the API is micro-milled to an exact, mathematically defined micron size to guarantee a highly predictable, extended dissolution profile in the gut, preventing toxic “dose dumping”) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict chronic neurology dispensing regimens and therapeutic drug monitoring protocols).
Disulfiram Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). The tablets are formulated to dissolve rapidly to ensure quick systemic coverage.
Active Ingredient Strength (Standard) Role Disulfiram USP/BP 250 mg Standard Maintenance Disulfiram USP/BP 500 mg Induction Dose Excipients Q.S. Microcrystalline Cellulose / Starch Divalproex Sodium Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the intensely hygroscopic active ingredient.
Active Ingredient Strength Primary Clinical Function Divalproex Sodium USP/Ph.Eur. 250 mg (DR / ER) The Titration & Pediatric Standard: The definitive unit utilized for careful initial dose titration in adult bipolar patients or weight-based dosing for pediatric epilepsy. Divalproex Sodium USP/Ph.Eur. 500 mg (DR / ER) The Neurology Macrodose: Massive therapeutic payload utilized for the aggressive, sustained suppression of chronic complex partial seizures and acute bipolar mania. Excipients (Enteric DR Formulation) Microcrystalline Cellulose / Croscarmellose Sodium / Povidone / Methacrylic Acid Copolymer (Eudragit) / Triethyl Citrate / Titanium Dioxide Diluent / Superdisintegrant / Binder / Enteric Polymer / Plasticizer / Opaque Film (Engineered specifically utilizing advanced fluid-bed enteric coating to completely shield the highly corrosive valproate compound from the stomach, ensuring the pill only dissolves in the alkaline environment of the small intestine to prevent severe gastric bleeding and vomiting) *Pack Sizes: 10×10 Alu-Alu Blisters or Heavy-Gauge HDPE Bottles (Optimized specifically for strict chronic neurology and psychiatry dispensing regimens).
Dolutegravir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Polymorphically Stabilized Microdose Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the Dolutegravir Sodium salt.
Active Ingredient Strength Primary Clinical Function Dolutegravir (as Sodium) USP/Ph.Eur. 50 mg The Global INSTI Anchor: The definitive therapeutic payload required to force immediate, systemic viral suppression and maintain an undetectable viral load. Excipients D-Mannitol / Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Sodium Stearyl Fumarate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing strict low-moisture granulation to prevent the active Dolutegravir Sodium from undergoing polymorphic shifts during compression, guaranteeing absolute pharmacokinetic bioequivalence) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 or 10×10 Alu-Alu Blisters (Optimized specifically for massive NGO distribution and chronic daily dispensing regimens).
Domperidone & Famotidine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Release FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Domperidone Maleate USP/Ph.Eur. 10 mg The Antiemetic/Prokinetic Anchor: The micro-dose peripheral D2 antagonist required to halt nausea and rapidly accelerate gastric emptying. Famotidine USP/Ph.Eur. 20 mg The Acid Suppressor (NDMA-Free): The highly potent, structurally stable H2-receptor antagonist required to crush basal and food-stimulated gastric acid secretion. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced rapid-burst disintegrants to ensure the tablet dissolves instantly in the stomach for fast relief, heavily coated to protect the APIs from environmental degradation) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for high-volume, rapid-turnover acute GI dispensing).
Domperidone & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Domperidone Maleate USP/Ph.Eur. 10 mg The Antiemetic/Prokinetic Anchor: The micro-dose peripheral D2 antagonist required to halt vomiting and rapidly accelerate gastric emptying. Paracetamol (Acetaminophen) USP/Ph.Eur. 500 mg The Central Analgesic Payload: The massive therapeutic payload required to elevate the central pain threshold and crush acute migraine pain. Excipients Microcrystalline Cellulose / Crospovidone / Maize Starch / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the massive 510mg active core shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the bitter taste of the APIs) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid-response outpatient pain management and acute neurology dispensing).
Domperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Release / MD Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability and instantaneous dissolution of the active ingredient.
Active Ingredient Strength Primary Clinical Function Domperidone Maleate USP/Ph.Eur. 10 mg The Global Antiemetic Standard: The definitive rapid-acting unit utilized globally for the immediate suppression of acute nausea and the acceleration of delayed gastric emptying. Excipients (MD Formulation) Microcrystalline Cellulose / Crospovidone / Mannitol / Aspartame / Peppermint Flavor / Magnesium Stearate Diluent / Superdisintegrant / Cooling Agent / Sweetener / Flavoring (Engineered specifically using elite “Rapid-Burst” superdisintegrants to ensure the Mouth Dissolving tablet shatters in saliva within seconds. This is critical because a vomiting patient physically cannot swallow water or a hard pill without instantly throwing it back up) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, short-term gastrointestinal dispensing regimens).
Donepezil Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White for 5mg and Yellow for 10mg). The film coating aids in swallowing and identification.
Active Ingredient Strength (Standard) Role Donepezil HCl USP/BP 5 mg Initial Titration Dose Donepezil HCl USP/BP 10 mg Standard Maintenance Dose Donepezil HCl USP/BP 23 mg High Dose (Sustained Release – Special Order) Excipients Q.S. Lactose Monohydrate / Starch Doripenem Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Doripenem Monohydrate USP/BP Equivalent to 500 mg Doripenem Standard Adult Dose Doripenem Monohydrate USP/BP Equivalent to 250 mg Renal Impairment Excipients None (Pure Sterile Powder) – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Dothiepin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Heavy-Coated Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure absolute chemical stability and patient safety.
Active Ingredient Strength Primary Clinical Function Dothiepin (Dosulepin) Hydrochloride USP/Ph.Eur. 25 mg The Titration & Geriatric Standard: The definitive low-dose unit utilized for careful initial titration, daytime anxiety management, or for elderly patients highly sensitive to anticholinergic side effects. Dothiepin (Dosulepin) Hydrochloride USP/Ph.Eur. 75 mg The Nighttime Maintenance Macrodose: High-efficacy therapeutic payload utilized strictly at bedtime to induce heavy sleep and drive profound, long-term monoamine receptor down-regulation. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Maize Starch / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opaque Polymeric Film Diluent / Binder / Disintegrant / Glidant / Heavy Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. Dothiepin hydrochloride is profoundly bitter and can cause local oral anesthesia if it dissolves in the mouth; our elite coating guarantees seamless swallowing and zero taste disruption) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, heavily monitored 30-day psychiatric dispensing regimens).
Doxepin Hydrochloride Capsules
FreeDoxepin Hydrochloride capsules are tricyclic antidepressants (TCAs) used to treat depression, anxiety, and sleep disorders (insomnia).
Doxofylline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the xanthine derivative.
Active Ingredient Strength Primary Clinical Function Doxofylline USP/Ph.Eur. 400 mg The Global Pulmonology Standard: The definitive therapeutic macrodose utilized globally for the rapid and sustained reversal of severe bronchoconstriction in adult asthma and COPD patients. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced rapid-burst disintegrants to ensure the massive 400mg tablet dissolves quickly in the stomach, while the heavy film-coat completely masks the intensely bitter taste characteristic of all xanthine alkaloids) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict chronic respiratory dispensing regimens).
Doxycycline 100mg Capsules
FreeDoxycycline 100mg capsules are broad-spectrum tetracycline antibiotics used for bacterial infections, malaria prophylaxis, and severe acne.
Doxycycline Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in amber glass vials.
Active Ingredient Strength Primary Use Doxycycline Hyclate USP/BP Equivalent to 100 mg Doxycycline Standard Adult Dose Excipients Ascorbic Acid / Mannitol Stabilizer / Bulking Agent *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Doxycycline Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets or Dispersible Tablets. The film coating is essential to prevent esophageal irritation.
Active Ingredient Strength (Standard) Primary Role Doxycycline Hyclate USP/BP 100 mg Standard Adult Dose Doxycycline Monohydrate USP/BP 100 mg Esophageal Safety Variant Excipients Q.S. Microcrystalline Cellulose / Titanium Dioxide Doxylamine Succinate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Release Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the succinate salt.
Active Ingredient Strength Primary Clinical Function Doxylamine Succinate USP/Ph.Eur. 25 mg The Global OTC Sleep Standard: The definitive therapeutic unit utilized globally for the immediate induction of sleep in patients suffering from transient or short-term insomnia. Excipients Microcrystalline Cellulose / Dibasic Calcium Phosphate / Sodium Starch Glycolate / Magnesium Stearate / Premium Polymeric Film Diluent / Densifier / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered specifically utilizing a dense, rapid-dissolving polymeric film to completely mask the notoriously bitter, metallic taste of the succinate salt, while guaranteeing the tablet shatters in the stomach within minutes for fast sleep onset) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for high-volume, over-the-counter retail distribution).
Dried Aluminium Hydroxide & Magnesium Trisilicate Tablet
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (Mint or Orange Flavor) to ensure rapid disintegration and palatability.
Active Ingredient Strength (Standard) Role Dried Aluminium Hydroxide Gel IP/BP/USP 250 mg Acid Neutralizer / Constipating Agent Magnesium Trisilicate IP/BP/USP 500 mg Acid Neutralizer / Adsorbent Excipients Q.S. Sweeteners / Flavoring Agents Dried Aluminium Hydroxide Gel, Magnesium Hydroxide & Dimethylpolysiloxane Tablets
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (typically White or Pink, Mint/Orange Flavored). The chewable format is critical for increasing the surface area for acid neutralization and gas dispersion.
Active Ingredient Strength (Standard) Therapeutic Role Dried Aluminium Hydroxide Gel USP/BP 250 mg / 400 mg Sustained Antacid Magnesium Hydroxide USP/BP 250 mg / 400 mg Rapid Antacid Activated Dimethylpolysiloxane (Simethicone) USP/BP 50 mg / 25 mg Antiflatulent (Gas Relief) Excipients Q.S. Mannitol / Sorbitol / Flavor Sweetener / Coolant Dried Aluminium Hydroxide Gel, Magnesium Trisilicate & Peppermint Oil Tablets
FreeProduct Composition & Strength
We supply this product as Chewable Tablets (typically White, Round, Mint-Flavored). The chewable format is essential to increase the surface area for rapid acid neutralization.
Active Ingredient Strength (Standard) Therapeutic Role Dried Aluminium Hydroxide Gel USP/BP 250 mg Antacid / Adsorbent Magnesium Trisilicate USP/BP 500 mg Antacid / Mucosal Protectant Peppermint Oil USP/BP Q.S. (e.g., 2-5 mg) Carminative / Flavor Excipients Q.S. Mannitol / Sucrose / Menthol Sweetener / Coolant Dried 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. Dried Ferrous Sulfate & Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Red or Brown). The coating masks the metallic taste and protects the iron from oxidation.
Active Ingredient Strength (Standard) Therapeutic Role Dried Ferrous Sulfate USP/BP 200 mg (Eq. to 65 mg Elemental Iron) Standard WHO Prophylaxis Dried Ferrous Sulfate USP/BP 335 mg (Eq. to 100 mg Elemental Iron) Therapeutic / Treatment Dose Folic Acid USP/BP 0.4 mg / 0.5 mg / 1.5 mg DNA Synthesis / Neural Tube Protection Excipients Q.S. Maize Starch / Titanium Dioxide / Red Oxide Disintegrant / Colorant Dried Ferrous Sulphate, Elemental Iron, Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Red, Brown, or Maroon). The coating acts as an oxidation barrier.
Active Salt Equivalent Elemental Iron Therapeutic Role Dried Ferrous Sulphate IP/BP 200 mg 65 mg Elemental Iron WHO Standard Prophylaxis Dried Ferrous Sulphate IP/BP 335 mg 100 mg Elemental Iron Therapeutic Anemia Treatment Folic Acid IP/BP 0.4 mg / 0.5 mg / 1.5 mg Neural Tube Protection Excipients Q.S. Cellulose / Titanium Dioxide / Oxide Colors Filler / Colorant Drotaverine & Aceclofenac Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Drotaverine Hydrochloride USP/Ph.Eur. 80 mg The Spasmolytic Anchor (Forte Dose): The massive isoquinoline payload required to rapidly force smooth muscle relaxation in the ureters, biliary tract, and uterus. Aceclofenac USP/Ph.Eur. 100 mg The Anti-Inflammatory Payload: The potent COX-2 preferential NSAID required to crush the radiating inflammatory pain and tissue swelling. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Enteric-Like Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing Bi-Layer Compression Technology to physically separate the two highly reactive APIs, guaranteeing maximum shelf-life and ensuring rapid, simultaneous gastric dissolution without the APIs degrading each other) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, short-term acute emergency dispensing regimens).
Drotaverine & Mefenamic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Bi-Layer Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Drotaverine Hydrochloride USP/Ph.Eur. 80 mg The Spasmolytic Anchor (Forte Dose): The massive isoquinoline payload required to rapidly force smooth muscle relaxation in the uterus, biliary tract, and intestines. Mefenamic Acid USP/Ph.Eur. 250 mg The Gynecological Analgesic Payload: The potent, dual-action fenamate NSAID required to crush radiating inflammatory pain and block uterine prostaglandin receptors. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Enteric-Like Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Heavy Film-Coating (Engineered specifically utilizing Bi-Layer Compression Technology to physically separate the two active APIs, guaranteeing maximum shelf-life and ensuring rapid gastric dissolution without the APIs chemically degrading each other) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute gynecological and emergency dispensing regimens).
Drotaverine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Drotaverine Hydrochloride USP/BP 40 mg 2 ml Ampoule (20 mg/ml) Excipients Sodium Metabisulfite Antioxidant *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Drotaverine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly bitter hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Drotaverine Hydrochloride USP/Ph.Eur. 40 mg The Standard GI/Gynecology Anchor: The definitive therapeutic unit utilized for irritable bowel syndrome (IBS), routine dysmenorrhea, and mild gastrointestinal cramping. Drotaverine Hydrochloride USP/Ph.Eur. 80 mg (Forte) The Acute Colic Macrodose: Massive therapeutic payload utilized for the immediate, aggressive suppression of agonizing renal colic (kidney stones), biliary colic (gallstones), and severe cervical spasms during labor. Excipients Lactose Monohydrate / Maize Starch / Crospovidone / Talc / Magnesium Stearate / Premium Polymeric Film Diluent / Disintegrant / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the tablet shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the intense, bitter taste of the API) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid-response acute ward dispensing and outpatient pain management).
Duloxetine Capsules
FreeDuloxetine capsules are delayed-release (gastro-resistant) medications used to treat depression, anxiety, and chronic pain. Because the medicine can be destroyed by stomach acid, it is formulated as acid-resistant pellets inside a hard gelatin capsule.
Duloxetine Tablets
FreeProduct Composition & Strength
We supply this product as Gastro-Resistant Tablets or Delayed-Release Capsules (containing enteric-coated pellets). Both forms ensure optimal bioavailability.
Active Ingredient Strength (Standard) Primary Role Duloxetine HCl USP/BP 20 mg Geriatric / Initial Dose Duloxetine HCl USP/BP 30 mg Standard Maintenance (Pain/Anxiety) Duloxetine HCl USP/BP 40 mg High Strength (Specific Mkts) Duloxetine HCl USP/BP 60 mg High Strength (Depression/Neuropathy) Dutasteride Capsules
FreeDutasteride capsules are most commonly available as 0.5 mg soft gelatin capsules. They contain the active drug dissolved in a liquid medium to ensure proper absorption
Dydrogesterone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the retro-steroidal API.
Active Ingredient Strength Primary Clinical Function Dydrogesterone USP/Ph.Eur. 10 mg The Global Fertility & Maternal Standard: The definitive therapeutic unit utilized globally for luteal phase support, miscarriage prevention, and chronic endometriosis management. Excipients Lactose Monohydrate / Hypromellose / Maize Starch / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Disintegrant / Glidant / Heavy Film-Coating (Engineered specifically utilizing high-shear wet granulation to ensure the 10mg steroidal payload is flawlessly uniform, finished with an opaque film-coat to lock the teratogen/hormone safely away from factory handlers) *Pack Sizes: 10×10 Blisters or Calendar Blisters of 14/28 (Optimized specifically for precise tracking during the menstrual cycle and IVF protocols).
Ebastine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Dissolution Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the piperidine derivative API.
Active Ingredient Strength Primary Clinical Function Ebastine USP/Ph.Eur. 10 mg The Standard Allergy Anchor: The definitive once-daily unit utilized for the baseline control of Seasonal and Perennial Allergic Rhinitis (Hay Fever). Ebastine USP/Ph.Eur. 20 mg The Dermatology Macrodose: High-efficacy therapeutic payload utilized strictly for severe, refractory Chronic Idiopathic Urticaria (hives) or intensely severe allergic rhinitis. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered utilizing elite rapid-burst disintegrants to ensure the tablet dissolves instantly in gastric fluid, expediting the hepatic conversion to Carebastine for the fastest possible onset of clinical relief) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, 30-day chronic allergy and dermatology dispensing regimens).
Efavirenz ,Emtricitabine & Tenofovir Disoproxil Fumarate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Mega-Dose FDC Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles to ensure the absolute chemical survival of the moisture-sensitive Tenofovir and light-sensitive Efavirenz.
Active Ingredient Strength Primary Clinical Function Efavirenz USP/Ph.Eur. 600 mg The NNRTI Anchor: The massive, highly lipophilic non-nucleoside payload required to force immediate, systemic viral suppression. Emtricitabine (FTC) USP/Ph.Eur. 200 mg The Cytidine Analogue: Provides profound, long-acting intracellular viral suppression to reinforce the backbone. Tenofovir Disoproxil Fumarate (TDF) USP/Ph.Eur. 300 mg The Nucleotide Backbone: The heavy-hitting chain terminator required to completely halt viral DNA elongation. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Hydroxypropyl Cellulose / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Surfactant / Heavy Film-Coating (Engineered utilizing High-Compression Bi-Layer Technology to fuse 1,100mg of active API into a single, aerodynamically shaped tablet that remains easy for patients to swallow, heavily coated to lock out destructive tropical humidity) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for massive NGO distribution and strict 30-day chronic daily dispensing regimens).
Efavirenz Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the highly lipophilic active ingredient.
Active Ingredient Strength Primary Clinical Function Efavirenz USP/Ph.Eur. 600 mg The Global NNRTI Macrodose: The massive therapeutic payload required to force immediate, systemic viral suppression when combined with a dual-NRTI backbone. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Sodium Lauryl Sulfate / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Surfactant / Binder / Heavy Film-Coating (Engineered specifically utilizing powerful surfactants like Sodium Lauryl Sulfate to drastically increase the solubility of the notoriously lipophilic Efavirenz molecule, ensuring rapid and complete gastrointestinal absorption) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 or 10×10 Alu-Alu Blisters (Optimized specifically for massive NGO distribution and chronic daily dispensing regimens).
Elevat
FreeThe term Elevat most commonly refers to Elevat 20 Capsule, a prescription antidepressant. However, depending on the specific product name (such as “Elevat D”), it may contain entirely different active ingredients like vitamins
Emtricitabine & Tenofovir Disoproxil Fumarate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrolytically Shielded Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge HDPE bottles or Alu-Alu blister strips to ensure the absolute chemical survival of the moisture-sensitive Tenofovir.
Active Ingredient Strength Primary Clinical Function Emtricitabine (FTC) USP/Ph.Eur. 200 mg The Cytidine Analogue: Provides profound, long-acting intracellular viral suppression with an exceptionally favorable safety profile. Tenofovir Disoproxil Fumarate (TDF) USP/Ph.Eur. 300 mg
(Eq. to 245 mg Tenofovir Disoproxil)The Nucleotide Backbone: The heavy-hitting reverse transcriptase inhibitor required to anchor the ARV regimen and prevent viral breakthrough. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Lactose Monohydrate / Magnesium Stearate / Premium Polymeric Film (Opadry) Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing dry-granulation and heavy film-coating to protect the API from atmospheric moisture, ensuring the massive 500mg active payload remains structurally intact and easily swallowable) *Pack Sizes: Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for massive NGO distribution and strict 30-day chronic daily dispensing regimens).
Enalapril Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration). The wide range of strengths allows for the “Start Low, Go Slow” dosing strategy essential for heart failure.
Active Ingredient Strength (Standard) Primary Role Enalapril Maleate USP/BP 2.5 mg Heart Failure Initiation Enalapril Maleate USP/BP 5 mg Hypertension Initiation Enalapril Maleate USP/BP 10 mg Maintenance Dose Enalapril Maleate USP/BP 20 mg High Strength Enoxaparin Injection
FreeEnoxaparin Sodium injection (brand name Lovenox) is a sterile, clear, colourless to pale yellow aqueous solution of a low molecular weight heparin (LMWH). It is primarily used to prevent and treat deep vein thrombosis (DVT) and pulmonary embolism.
Active IngredientStrengthTherapeutic RoleEnoxaparin Sodium USP/BP40 mg / 0.4 mlProphylaxis (DVT Prevention)Enoxaparin Sodium USP/BP60 mg / 0.6 mlTreatment (Weight Adjusted)Enoxaparin Sodium USP/BP80 mg / 0.8 mlTreatment (DVT/PE/ACS)OriginPorcine MucosaViral Safety Certified
Entacavir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the potent antiviral API.
Active Ingredient Strength Primary Clinical Function Entecavir (as Monohydrate) USP/Ph.Eur. 0.5 mg The Global Nucleoside-Naive Standard: The definitive ultra-micro-dose utilized for the daily, lifelong suppression of HBV in patients who have never received prior antiviral therapy. Entecavir (as Monohydrate) USP/Ph.Eur. 1.0 mg The Refractory & Cirrhosis Standard: Double-strength therapeutic payload utilized specifically for patients with Lamivudine-resistant HBV viremia or those suffering from decompensated liver cirrhosis. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the microscopic 0.5mg payload is flawlessly distributed throughout the tablet matrix, preventing toxic “hot spots” or sub-therapeutic failures) *Pack Sizes: 3×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic hepatology dispensing regimens).
Epalrestat Sustained Release Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable SR Matrix Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the intensely photolabile molecule.
Active Ingredient Strength Primary Clinical Function Epalrestat USP/Ph.Eur. 150 mg (SR) The Global Diabetology Standard: The definitive macrodose engineered for 24-hour continuous aldose reductase suppression, dramatically improving patient adherence over standard 50mg TID dosing. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Titanium-Dioxide Film Rate-Controlling Polymer / Diluent / Glidant / Lubricant / UV-Barrier Film (Engineered utilizing elite viscosity-grade HPMC to form a gel-matrix in the gut for sustained drug release, finished with a heavy, opaque film-coat to act as an absolute UV/Light barrier) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic diabetic dispensing regimens).
Ergometrine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets. The coating is critical to protect the active ingredient from oxidation and light.
Active Ingredient Strength (Standard) Primary Role Ergometrine Maleate USP/BP 0.2 mg (200 mcg) PPH Prevention / Subinvolution Ergometrine Maleate USP/BP 0.5 mg (500 mcg) High Potency (Specific Mkts) Excipients Q.S. Tartaric Acid (Stabilizer) Ergotamine & Caffeine ,Paracetamol & Prochlorperazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Quad-API Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive ergot alkaloid and phenothiazine components.
Active Ingredient Strength Primary Clinical Function Ergotamine Tartrate USP/Ph.Eur. 1 mg The Vascular Terminator (Micro-Dose): The foundational ergot alkaloid required to aggressively constrict pulsing cranial arteries. Caffeine Anhydrous USP/Ph.Eur. 100 mg The Absorption Catalyst: Enhances Ergotamine bioavailability and accelerates onset of action. Paracetamol (Acetaminophen) USP/Ph.Eur. 250 mg The Central Analgesic (Macro-Dose): Provides immediate, broad-spectrum relief from accompanying head and neck pain. Prochlorperazine Maleate USP/Ph.Eur. 2.5 mg The Antiemetic Anchor (Ultra-Micro-Dose): Lethally blocks the CTZ to prevent vomiting and ensure full gastrointestinal absorption of the FDC. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant (Engineered utilizing extreme multi-stage geometric dilution to flawlessly blend a microscopic 1mg and 2.5mg payload into a massive 250mg/100mg base, guaranteeing absolute content uniformity and zero toxic ‘hot spots’) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, heavily limited acute neurology dispensing to prevent ergot toxicity).
Erlotinib Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the targeted antineoplastic API.
Active Ingredient Strength Primary Clinical Function Erlotinib (as Hydrochloride) USP/Ph.Eur. 100 mg The Pancreatic Oncology Standard: The definitive daily maintenance dose utilized globally in combination with Gemcitabine for advanced, unresectable, or metastatic pancreatic cancer. Erlotinib (as Hydrochloride) USP/Ph.Eur. 150 mg The Thoracic Oncology Standard: Massive therapeutic payload utilized as a first-line, maintenance, or second-line daily monotherapy for EGFR-mutated Non-Small Cell Lung Cancer. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to maximize dissolution of this highly insoluble compound while locking the potent cytotoxic API safely inside the tablet, completely preventing handler exposure to carcinogenic dust) *Pack Sizes: 3×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Erythromycin Capsules
FreeErythromycin capsules are macrolide antibiotics used to treat various bacterial infections. Because erythromycin base is easily destroyed by stomach acid, these capsules are typically formulated as delayed-release systems containing enteric-coated pellets
Erythromycin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Pink/Red). The coating is essential to mask the intensely bitter taste of the API.
Active Ingredient Strength (Standard) Primary Role Erythromycin Stearate USP/BP
(Equivalent to Erythromycin Base)250 mg Pediatric / Mild Infection Erythromycin Stearate USP/BP
(Equivalent to Erythromycin Base)500 mg Adult Standard Dose Excipients Q.S. Maize Starch / Povidone Erythropoietin Prefilled Syringe Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid in a Prefilled Syringe (PFS) with a fine needle.
Active Ingredient Strength (IU) Patient Profile Recombinant Human Erythropoietin 2000 IU / 0.5 ml Maintenance / Low Weight Recombinant Human Erythropoietin 4000 IU / 0.4 ml Standard Dialysis Dose Recombinant Human Erythropoietin 10000 IU / 1.0 ml Chemotherapy / High Dose Stabilizer Human Albumin / Polysorbate Prevents Protein Aggregation *Pack Sizes: Blister Pack of 1 PFS or Box of 6 PFS.
Escitalopram Oxalate & Clonazepam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Escitalopram (as Oxalate) USP/Ph.Eur. 5 mg / 10 mg The Serotonin Anchor (Macro-Dose): The foundational, highly selective SSRI required to cure the underlying clinical depression and generalized anxiety. Clonazepam USP/Ph.Eur. 0.25 mg / 0.5 mg The Anxiolytic Bridge (Micro-Dose): The highly potent, long-acting benzodiazepine required to suppress acute panic attacks and SSRI-induced activation syndrome. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 0.25mg/0.5mg micro-dose of Clonazepam is flawlessly distributed throughout the Escitalopram matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 2-to-4 week short-term bridging regimens before stepping down to Escitalopram monotherapy).
Esomeprazole & Levosulpiride Capsules
FreeEsomeprazole and Levosulpiride capsules are a combination medication primarily used for gastroesophageal reflux disease (GERD) and peptic ulcers in patients who do not respond to a proton pump inhibitor (PPI) alone.
Esomeprazole Capsule
FreeEsomeprazole capsules primarily contain Esomeprazole Magnesium (as a dihydrate or trihydrate) as the active ingredient. Because esomeprazole is “acid-labile” (broken down by stomach acid), these capsules are formulated as delayed-release or gastro-resistant systems containing enteric-coated pellets.
Esomeprazole Domperidone Capsules
FreeEsomeprazole and Domperidone capsules are combination medications containing two active pharmaceutical ingredients, typically formulated as pellets within a hard gelatin capsule.
Esomeprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Form Esomeprazole Sodium USP/BP Equivalent to 40 mg Esomeprazole White to Off-White Cake Excipients Disodium Edetate / Sodium Hydroxide Chelating Agent / pH Adjuster *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Esomeprazole Tablets
FreeProduct Composition & Strength
We supply this product as Gastro-Resistant (Enteric Coated) Tablets. The drug is acid-labile and must pass through the stomach intact to be absorbed in the intestine.
Active Ingredient Strength (Standard) Role Esomeprazole Magnesium Trihydrate USP/BP 20 mg Maintenance / Mild GERD Esomeprazole Magnesium Trihydrate USP/BP 40 mg Erosive Esophagitis / Zollinger-Ellison Excipients Q.S. Enteric Polymers (Methacrylic Acid) Estramustine Phosphate Capsules
FreeEstramustine phosphate capsules typically contain estramustine phosphate sodium as the active medicinal ingredient, along with several inactive excipients to ensure the drug’s stability and delivery.
Ethambutol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often Gray or White). Coating is essential as the API is hygroscopic and has a bitter taste.
Active Ingredient Strength (Standard) Primary Role Ethambutol HCl USP/BP/IP 200 mg Pediatric / Renal Adjustment Ethambutol HCl USP/BP/IP 400 mg Standard Adult Unit Ethambutol HCl USP/BP/IP 600 mg High Strength (Daily Regimen) Ethambutol HCl USP/BP/IP 800 mg Intensive Phase Loading Ethambutol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential as Ethambutol HCl is highly hygroscopic (absorbs moisture) and has a bitter taste.
Active Ingredient Strength (Standard) Role in DOTS Therapy Ethambutol HCl USP/BP 200 mg Pediatric / Renal Adjustment Ethambutol HCl USP/BP 400 mg Standard Adult Unit Ethambutol HCl USP/BP 600 mg / 800 mg High Weight Band / Forte Ethambutol HCl USP/BP 1000 mg High Dose (Special Order) Excipients Q.S. Sorbitol / Magnesium Stearate Ethamsylate tablets
FreeAn Ethamsylate tablet is a hemostatic (antihemorrhagic) medication used to prevent and control excessive bleeding, particularly from small blood vessels (capillaries).
Ethamsylate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Oxidation-Resistant Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical survival of the highly reactive active ingredient.
Active Ingredient Strength Primary Clinical Function Ethamsylate USP/Ph.Eur. 250 mg The Prophylactic Surgical Standard: Base therapeutic unit utilized for pre-operative dosing to prevent excessive capillary oozing during delicate ENT (tonsillectomy) or dental procedures. Ethamsylate USP/Ph.Eur. 500 mg The Acute Gynecology Macrodose: Massive therapeutic payload utilized for the aggressive, immediate suppression of severe menorrhagia (heavy menstrual bleeding) and acute trauma. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K-30 / Sodium Metabisulfite / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Antioxidant / Film-Coating (Engineered specifically incorporating powerful antioxidants and a heavy moisture-barrier film to completely shield the API from atmospheric oxygen, preventing the tablet from degrading and turning black/pink on the shelf) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 5-to-10 day acute surgical and gynecological dispensing regimens).
Ethinyestradiol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hazard-Shielded Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the synthetic steroidal API.
Active Ingredient Strength Primary Clinical Function Ethinylestradiol USP/Ph.Eur. 0.05 mg (50 mcg) The Endocrinology Standard: The definitive micro-dose engineered specifically for female hypogonadism, primary ovarian failure, and strictly monitored estrogen replacement. Ethinylestradiol USP/Ph.Eur. 1 mg The Palliative Oncology Macrodose: Massive therapeutic payload utilized strictly for the aggressive hormonal suppression of advanced, inoperable prostate or breast cancer. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / Heavy Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. This completely seals the potent steroidal API, ensuring absolute safety for handlers and guaranteeing zero cross-contamination in the facility) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict chronic endocrine and oncology dispensing regimens).
Ethinylestradiol & Levonorgestrel Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant “Calendar Blister” packs to ensure absolute daily patient compliance and chemical stability.
Active Ingredient Strength Primary Clinical Function Ethinylestradiol USP/Ph.Eur. 0.03 mg (30 mcg) The Estrogenic Anchor: The synthetic estrogen required to suppress FSH release and stabilize the uterine lining to prevent irregular breakthrough bleeding. Levonorgestrel USP/Ph.Eur. 0.15 mg (150 mcg) The Progestin Powerhouse: The highly potent, second-generation progestin required to suppress the LH surge and thicken the cervical mucus. Excipients Lactose Monohydrate / Maize Starch / Povidone K-30 / Magnesium Stearate / Premium Sugar/Film Coating Diluent / Disintegrant / High-Shear Binder / Lubricant (Engineered specifically using elite multi-stage geometric dilution to guarantee the microscopic 30 mcg and 150 mcg payloads are flawlessly distributed, preventing lethal hormonal drops that cause contraceptive failure) *Pack Sizes: 21-Day Active Blisters OR 28-Day Calendar Blisters (21 Active Hormonal Tablets + 7 Placebo/Iron Tablets to enforce daily habit-forming compliance).
Ethionamide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Yellow/Orange). Effective coating is mandatory as the drug causes significant gastric irritation and has a metallic taste.
Active Ingredient Strength (Standard) Target Patient Ethionamide USP/BP/IP 250 mg Standard Adult / Pediatric Unit Excipients Q.S. Microcrystalline Cellulose / Hypromellose Etizolam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the ultra-low-dose API.
Active Ingredient Strength Primary Clinical Function Etizolam JP/Ph.Eur. 0.25 mg The Geriatric & Daytime Standard: The definitive ultra-low-dose unit utilized for daytime anxiety suppression without severe sedation, or for highly sensitive elderly patients. Etizolam JP/Ph.Eur. 0.5 mg / 1 mg The Panic & Insomnia Standard: High-efficacy therapeutic payload utilized for the immediate termination of acute panic attacks and the induction of sleep in severe insomnia. Excipients (MD Formulation) Mannitol / Crospovidone / Aspartame / Peppermint Flavor / Magnesium Stearate Diluent / Superdisintegrant / Sweetener / Flavoring (Engineered specifically using elite “Rapid-Burst” superdisintegrants to ensure the tablet shatters and dissolves in saliva within seconds, masking the chemical taste for maximum patient compliance during severe distress) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, short-term psychiatric dispensing regimens).
Etmsylate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules.
Active Ingredient Strength Volume Etamsylate USP/BP 250 mg 2 ml Ampoule (125 mg/ml) – Standard Etamsylate USP/BP 125 mg 2 ml Ampoule – Pediatric Excipients Sodium Metabisulfite Antioxidant *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Etofylline Theophylline Tablets
FreeProduct Composition & Strength
We supply this product as Prolonged Release (PR/Retard) Tablets or standard Film Coated Tablets.
Formulation Variant Etofylline Strength Theophylline Strength Total Potency Role Standard Tablet 77 mg 23 mg 100 mg Acute / Pediatric Retard 150 115 mg 35 mg 150 mg Mild Maintenance Retard 300 231 mg 69 mg 300 mg Adult Standard (BID) Retard 450 346.5 mg 103.5 mg 450 mg High Dose (OD) Etoricoxib Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (distinctively colored by strength). The coating masks the bitter taste and ensures stability.
Active Ingredient Strength (Standard) Color (Typical) Primary Indication Etoricoxib USP/BP 60 mg Green Osteoarthritis / Chronic Pain Etoricoxib USP/BP 90 mg White Rheumatoid Arthritis / Dental Pain Etoricoxib USP/BP 120 mg Pale Green Acute Gout (Short Term) Everolimus Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Antioxidant-Stabilized Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the highly oxidative, potent API.
Active Ingredient Strength Primary Clinical Function Everolimus USP/Ph.Eur. 0.25 mg / 0.5 mg / 0.75 mg Global Transplant Standard: Ultra-micro doses utilized for strict, lifelong immunosuppression following renal or hepatic allografts. Requires extreme content uniformity to maintain the narrow therapeutic blood trough levels (3 to 8 ng/mL). Everolimus USP/Ph.Eur. 5 mg / 10 mg Global Oncology Standard: Massive-dose antineoplastic payload utilized for the aggressive suppression of Renal Cell Carcinoma, Neuroendocrine Tumors (NETs), and HR+/HER2- Breast Cancer. Excipients Butylated Hydroxytoluene (BHT) / Hypromellose / Lactose Anhydrous / Crospovidone / Magnesium Stearate Antioxidant / Binder / Diluent / Superdisintegrant / Lubricant (Engineered specifically utilizing BHT (Butylated Hydroxytoluene) to prevent the rapid oxidative degradation of the Everolimus molecule, guaranteeing maximum clinical shelf-life and potency across harsh climates) *Pack Sizes: 10×10 Alu-Alu Blisters (Transplant) or 3×10 Alu-Alu Blisters (Oncology – 30 Day Supply).
Exemestane Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the potent steroidal antineoplastic agent.
Active Ingredient Strength Primary Clinical Function Exemestane USP/Ph.Eur. 25 mg Global Adult Oncology Standard: The definitive daily maintenance dose required to maintain absolute, continuous destruction of peripheral aromatase enzymes and keep estrogen levels crashed. Excipients Mannitol / Copovidone / Crospovidone / Sodium Starch Glycolate / Magnesium Stearate / Premium Polymeric Film Diluent / High-Shear Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to lock the highly potent, teratogenic steroidal API safely inside the tablet, completely preventing handler and pharmacist exposure to the hazardous dust) *Pack Sizes: 10×10 Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Famotidine & Domperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density Alu-PVC blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Famotidine USP/Ph.Eur. 20 mg Global Clinical Standard: Safe, NDMA-free H2 antagonist for baseline acid suppression. Domperidone Maleate BP/Ph.Eur. 10 mg (Base Equivalent) Peripheral prokinetic and anti-emetic to accelerate gastric emptying and prevent reflux. Excipients Microcrystalline Cellulose / Maize Starch / Crospovidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Lubricant (Engineered for immediate gastric dissolution and synchronized absorption) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-turnover retail OTC and acute gastroenterology dispensing).
Famotidine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Square or Round). The film coating masks the bitter taste and protects the API from moisture.
Active Ingredient Strength (Standard) Role Famotidine USP/BP 20 mg GERD / Heartburn / Maintenance Famotidine USP/BP 40 mg Ulcer Healing / Hypersecretory States Excipients Q.S. Starch (Disintegrant) / Hypromellose Favipiravir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the active pyrazinecarboxamide derivative.
Active Ingredient Strength Primary Clinical Function Favipiravir USP/Ph.Eur. 200 mg The Global Outbreak Standard: Base therapeutic unit utilized for standard, highly flexible titration during acute viral hemorrhagic fevers or novel influenza outbreaks. Favipiravir USP/Ph.Eur. 400 mg / 800 mg The Pill-Burden Reduction Macrodose: Massive therapeutic payload engineered specifically to solve the severe “Day 1 Loading Dose” compliance nightmare (allowing a patient to take two 800mg pills instead of eight 200mg pills). Excipients Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Colloidal Silicon Dioxide / Sodium Stearyl Fumarate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Lubricant (Engineered specifically utilizing advanced high-shear wet granulation to compress massive, bulky API doses into smooth, easily swallowable tablets, finished with a heavy film-coat to lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters or Complete Therapy “Outbreak Kits” (e.g., 34-tablet or 40-tablet regimen boxes).
Ferrous Acorbate & Folic acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Hematinic FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive iron complex.
Active Ingredient Strength Primary Clinical Function Ferrous Ascorbate USP/Ph.Eur.
(Equivalent to Elemental Iron)100 mg The Hemoglobin Anchor: Massive, highly bioavailable elemental iron payload required to rapidly reverse severe maternal anemia without inducing dose-limiting gastric toxicity. Folic Acid (Vitamin B9) USP/Ph.Eur. 1.5 mg The DNA Synthesizer: Critical micro-dose required to drive red blood cell proliferation and guarantee fetal neurodevelopmental safety. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered specifically using a heavy, dark-colored polymeric film-coat to completely mask the violent, metallic taste of the iron and prevent the tablet from rapidly oxidizing on the shelf) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, daily 9-month prenatal dispensing regimens).
Ferrous Folic Tablets
FreeProduct Composition & Strength
We supply this product primarily as Sugar Coated Tablets (Red/Maroon) to mask the metallic taste, or Film Coated Tablets.
Component Strength (Standard) Strength (Therapeutic) Role Dried Ferrous Sulphate 200 mg
(~60-65 mg Elemental Iron)200 mg
(~60-65 mg Elemental Iron)Hemoglobin Synthesis Folic Acid 0.4 mg (400 mcg) 1.5 mg / 5 mg DNA Synthesis / NTD Prevention Color Red / Maroon Red / Brown Identification Ferrous Fumarate with Folic Acid Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential to mask the metallic taste of iron and prevent the oxidation of the ferrous salt during storage.
Active Ingredient Strength (Standard) Therapeutic Role Ferrous Fumarate BP/USP 200 mg / 300 mg Hematinic (Iron Supplement) Folic Acid BP/USP 0.4 mg / 0.5 mg / 1 mg / 5 mg Vitamin B9 (Folates) Excipients Q.S. Povidone / Talc / Magnesium Stearate Stabilizing Core Matrix Ferrous Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. The sugar coating is critical to mask the strong, astringent metallic taste and prevent gastric nausea.
Active Ingredient Strength Elemental Iron Primary Role Dried Ferrous Sulphate USP/BP 200 mg ~ 65 mg Standard Adult Therapy Dried Ferrous Sulphate USP/BP 300 mg ~ 100 mg High Dose Treatment Excipients Q.S. Sucrose (Coating) / Talc Taste Masking Finasteride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hazard-Shielded Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Finasteride USP/Ph.Eur. 1 mg The Global Dermatology Standard: The definitive micro-dose engineered specifically for the lifelong, daily maintenance of Androgenetic Alopecia (Male Pattern Hair Loss). Finasteride USP/Ph.Eur. 5 mg The Global Urology Standard: High-efficacy macro-dose utilized for the aggressive shrinkage of the prostate gland in symptomatic Benign Prostatic Hyperplasia (BPH). Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Docusate Sodium / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Opadry Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. This completely seals the teratogenic API, ensuring absolute safety for female pharmacists and caregivers handling the medication) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for strict, lifelong chronic urology and dermatology dispensing regimens).
Flavoxate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Flavoxate Hydrochloride USP/Ph.Eur. 200 mg The Global Urological Standard: The definitive macrodose therapeutic unit utilized for rapid, acute suppression of agonizing bladder spasms and chronic overactive bladder maintenance. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the massive 200mg tablet shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the bitter taste) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-4 times daily acute dispensing regimens).
Flucloxacillin and Amoxicillin Capsules
FreeFlucloxacillin and amoxicillin combination capsules (often referred to by trade names like Flamox (cosmos-pharm.com) or Amoxam) contain two distinct penicillin-type antibiotics (hra.nhs.uk) that work together to treat a broader range of bacterial infections.
Flucloxacillin Capsules
FreeFlucloxacillin capsules contain flucloxacillin sodium as the active ingredient, along with specific excipients that vary slightly by manufacturer but typically include a lubricant, a glidant, and sodium.
Flucloxacillin Injection
FreeFlucloxacillin injection is a narrow-spectrum penicillin antibiotic used to treat infections caused by staphylococci. It is typically supplied as a white to off-white sterile powder for reconstitution.
Fluconazole & Ivermectin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Fluconazole USP/Ph.Eur. 150 mg The Antifungal Anchor (Macro-Dose): The foundational triazole payload required to systematically eradicate widespread dermatophytes and yeasts. Ivermectin EP/USP 6 mg / 12 mg The Antiparasitic Assassin (Micro-Dose): The highly potent, targeted neurotoxin required to paralyze burrowing mites, lice, and severe helminthic infections. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 6mg micro-dose of Ivermectin is flawlessly distributed throughout the massive Fluconazole matrix, preventing toxic “hot spots”) *Pack Sizes: Single-Dose Blister Packs (1×1 or 1×2) or 10×10 Blisters (Optimized specifically for rapid NGO deployment and “stat” dosing protocols).
Fluconazole Capsules
FreeFluconazole capsules (commonly known by the brand name Diflucan (pfizermedical.com)) contain the active antifungal ingredient fluoxetine hydrochloride along with a powder fill of inactive excipients and a hard gelatin shell.
