Showing 501–1000 of 1289 results
Enrofloxacin veterinary injection
FreeComposition
Enrofloxacin INJ. 50 ML
Usage: –It’s crucial to use enrofloxacin injections only under the guidance of a veterinarian
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
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. 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 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 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).
Ethamsylate tablets
FreeAn Ethamsylate tablet is a hemostatic (antihemorrhagic) medication used to prevent and control excessive bleeding, particularly from small blood vessels (capillaries).
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) Etophylline & Theophylline injection
FreeComposition
Each ml contains- Etophylline IP 84.7 mg + Theophylline
(anhydrous) eq. to Theophylline (hydrated)
25.3 mg + Benzyl alcohol ( as preservative )
0.2% v/v + WFI IP q.s INJECTION (2 ML)
Usage: – commonly used in the treatment of asthma
Category: – Pulmonary injection (COPD)
Therapeutic category: –Pulmonary Disease (COPD)
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
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).
Ferric Hydroxide injection
FreeComposition
Ferric Hydroxide (Iron) 20 mg INJ 1 X 5 ML
Usage: –it is commonly used to treat iron deficiency anemia
Category: – anemia injection
Therapeutic category: –deficiency anemia
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
Ferrous Acorbate & Folic acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Hematinic FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive iron complex.
Active Ingredient Strength Primary Clinical Function Ferrous Ascorbate USP/Ph.Eur.
(Equivalent to Elemental Iron)100 mg The Hemoglobin Anchor: Massive, highly bioavailable elemental iron payload required to rapidly reverse severe maternal anemia without inducing dose-limiting gastric toxicity. Folic Acid (Vitamin B9) USP/Ph.Eur. 1.5 mg The DNA Synthesizer: Critical micro-dose required to drive red blood cell proliferation and guarantee fetal neurodevelopmental safety. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered specifically using a heavy, dark-colored polymeric film-coat to completely mask the violent, metallic taste of the iron and prevent the tablet from rapidly oxidizing on the shelf) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, daily 9-month prenatal dispensing regimens).
Ferrous Folic Tablets
FreeProduct Composition & Strength
We supply this product primarily as Sugar Coated Tablets (Red/Maroon) to mask the metallic taste, or Film Coated Tablets.
Component Strength (Standard) Strength (Therapeutic) Role Dried Ferrous Sulphate 200 mg
(~60-65 mg Elemental Iron)200 mg
(~60-65 mg Elemental Iron)Hemoglobin Synthesis Folic Acid 0.4 mg (400 mcg) 1.5 mg / 5 mg DNA Synthesis / NTD Prevention Color Red / Maroon Red / Brown Identification Ferrous Fumarate with Folic Acid Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating is essential to mask the metallic taste of iron and prevent the oxidation of the ferrous salt during storage.
Active Ingredient Strength (Standard) Therapeutic Role Ferrous Fumarate BP/USP 200 mg / 300 mg Hematinic (Iron Supplement) Folic Acid BP/USP 0.4 mg / 0.5 mg / 1 mg / 5 mg Vitamin B9 (Folates) Excipients Q.S. Povidone / Talc / Magnesium Stearate Stabilizing Core Matrix Ferrous Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. The sugar coating is critical to mask the strong, astringent metallic taste and prevent gastric nausea.
Active Ingredient Strength Elemental Iron Primary Role Dried Ferrous Sulphate USP/BP 200 mg ~ 65 mg Standard Adult Therapy Dried Ferrous Sulphate USP/BP 300 mg ~ 100 mg High Dose Treatment Excipients Q.S. Sucrose (Coating) / Talc Taste Masking Finasteride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hazard-Shielded Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Finasteride USP/Ph.Eur. 1 mg The Global Dermatology Standard: The definitive micro-dose engineered specifically for the lifelong, daily maintenance of Androgenetic Alopecia (Male Pattern Hair Loss). Finasteride USP/Ph.Eur. 5 mg The Global Urology Standard: High-efficacy macro-dose utilized for the aggressive shrinkage of the prostate gland in symptomatic Benign Prostatic Hyperplasia (BPH). Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Docusate Sodium / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Opadry Film-Coating (Engineered specifically to form an impenetrable physical barrier over the tablet core. This completely seals the teratogenic API, ensuring absolute safety for female pharmacists and caregivers handling the medication) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for strict, lifelong chronic urology and dermatology dispensing regimens).
Flavoxate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Flavoxate Hydrochloride USP/Ph.Eur. 200 mg The Global Urological Standard: The definitive macrodose therapeutic unit utilized for rapid, acute suppression of agonizing bladder spasms and chronic overactive bladder maintenance. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced “Rapid-Burst” superdisintegrants to ensure the massive 200mg tablet shatters instantly upon contact with gastric fluid, guaranteeing hyper-fast pain relief while masking the bitter taste) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-4 times daily acute dispensing regimens).
Flucloxacillin and Amoxicillin Capsules
FreeFlucloxacillin and amoxicillin combination capsules (often referred to by trade names like Flamox (cosmos-pharm.com) or Amoxam) contain two distinct penicillin-type antibiotics (hra.nhs.uk) that work together to treat a broader range of bacterial infections.
Flucloxacillin Capsules
FreeFlucloxacillin capsules contain flucloxacillin sodium as the active ingredient, along with specific excipients that vary slightly by manufacturer but typically include a lubricant, a glidant, and sodium.
Flucloxacillin Injection
FreeFlucloxacillin injection is a narrow-spectrum penicillin antibiotic used to treat infections caused by staphylococci. It is typically supplied as a white to off-white sterile powder for reconstitution.
Fluconazole & Ivermectin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Fluconazole USP/Ph.Eur. 150 mg The Antifungal Anchor (Macro-Dose): The foundational triazole payload required to systematically eradicate widespread dermatophytes and yeasts. Ivermectin EP/USP 6 mg / 12 mg The Antiparasitic Assassin (Micro-Dose): The highly potent, targeted neurotoxin required to paralyze burrowing mites, lice, and severe helminthic infections. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 6mg micro-dose of Ivermectin is flawlessly distributed throughout the massive Fluconazole matrix, preventing toxic “hot spots”) *Pack Sizes: Single-Dose Blister Packs (1×1 or 1×2) or 10×10 Blisters (Optimized specifically for rapid NGO deployment and “stat” dosing protocols).
Fluconazole Capsules
FreeFluconazole capsules (commonly known by the brand name Diflucan (pfizermedical.com)) contain the active antifungal ingredient fluoxetine hydrochloride along with a powder fill of inactive excipients and a hard gelatin shell.
Fluconazole Tablets
FreeFLUCONAZOLE TABLETS IP 150 MG
Each uncoated tablet contains:
Fluconazole IP 150 mg Excipients q.s.Nuflucon – 200
Fluconazole Tablets IP 200 mg
Each Uncoated Tablet contains :
Fluconazole IP 200 mgUsage: – Prevent and treat a variety of fungal and yeast infections
Category: – Antifungal Drugs
Therapeutic category: – Antifungal
Fludac
FreeFludac is a brand name for capsules manufactured by Cadila Pharmaceuticals Ltd (amazon.in), used primarily as an antidepressant. It belongs to the class of Selective Serotonin Reuptake Inhibitors (SSRIs) (1mg.com).
Flunarazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the dihydrochloride salt.
Active Ingredient Strength Primary Clinical Function Flunarizine (as Dihydrochloride) USP/Ph.Eur. 5 mg The Pediatric & Geriatric Standard: The definitive low-dose unit required for migraine prophylaxis in children or for treating vertigo in elderly patients who are highly sensitive to drug accumulation. Flunarizine (as Dihydrochloride) USP/Ph.Eur. 10 mg The Global Adult Migraine Standard: High-efficacy adult maintenance dose utilized for maximum suppression of chronic, refractory migraine attacks. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant / Lubricant (Engineered utilizing elite low-dose geometric dilution to guarantee that the 5mg or 10mg micro-dose is flawlessly distributed, preventing accidental drug-accumulation spikes) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, heavily monitored 3-to-6 month neurology dispensing regimens).
Fluoxetine Capsules
FreeFluoxetine capsules, commonly known by the brand name Prozac (accessdata.fda.gov), contain the active antidepressant fluoxetine hydrochloride along with several inactive ingredients that vary by manufacturer and dosage strength.
Flupentixol & Melitracen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose FDC Tablet, packed exclusively in highly secure, light-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly photolabile thioxanthene derivative.
Active Ingredient Strength Primary Clinical Function Flupentixol (as Dihydrochloride) USP/Ph.Eur. 0.5 mg The Anxiolytic Activator (Ultra-Micro-Dose): The foundational presynaptic autoreceptor antagonist required to rapidly resolve apathy, fatigue, and physical tension. Melitracen (as Hydrochloride) USP/Ph.Eur. 10 mg The Mood Elevator (Micro-Dose): The highly tolerable TCA required to lift the baseline depressive neurosis. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Premium Opaque Polymeric Film Diluent / Binder / Superdisintegrant / Lubricant / UV-Barrier Film (Engineered utilizing elite multi-stage geometric dilution to guarantee the lethal 0.5mg micro-dose of Flupentixol is flawlessly distributed throughout the matrix, finished with a heavy, opaque coat to prevent UV degradation) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid-response, short-to-medium term psychiatric and general medicine dispensing regimens).
Fluphenazine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Amber Glass Ampoules or Vials.
Active Ingredient Strength Type Fluphenazine Decanoate USP/BP 25 mg 1 ml Ampoule / Vial Fluphenazine Decanoate USP/BP 12.5 mg 0.5 ml Ampoule (Starter Dose) Vehicle Sesame Oil Depot Base Preservative Benzyl Alcohol 1.5% v/v (In Vials) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 10 ml Multi-Dose Vial.
Flutamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the antiandrogen API.
Active Ingredient Strength Primary Clinical Function Flutamide USP/Ph.Eur. 250 mg Global Uro-Oncology Standard: The definitive therapeutic unit utilized for chronic, 8-hourly maintenance in Maximum Androgen Blockade (MAB) protocols. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to lock the potent antiandrogen API safely inside the tablet, completely preventing handler and pharmacist exposure to the hazardous hormonal dust) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, high-volume chronic oncology dispensing regimens).
Fluvoxamine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Scored Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the maleate salt.
Active Ingredient Strength Primary Clinical Function Fluvoxamine Maleate USP/Ph.Eur. 50 mg (Scored) Psychiatric Titration Standard: The definitive base unit required for the slow, highly monitored initiation of therapy to prevent severe nausea and activation syndrome in hyper-anxious patients. Fluvoxamine Maleate USP/Ph.Eur. 100 mg (Scored) Global OCD Maintenance Standard: High-efficacy adult maintenance dose. OCD frequently requires massive dosing (up to 300 mg/day), requiring dense, easily swallowable macrodose tablets. Excipients Mannitol / Microcrystalline Cellulose / Pregelatinized Starch / Sodium Stearyl Fumarate / Premium Hypromellose Film Diluent / Binder / Disintegrant / Lubricant / Slipper-Coating (Engineered specifically to compress the active API securely while utilizing a heavy, slick film-coat to completely mask the intensely bitter taste of Fluvoxamine, ensuring long-term patient compliance) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict 3-to-6 month chronic psychiatric dispensing regimens).
Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Yellow/Orange) in standard therapeutic and prophylactic strengths.
Active Ingredient Strength (Standard) Primary Role Folic Acid USP/BP 400 mcg (0.4 mg) Pre-conception / Prophylaxis Folic Acid USP/BP 1 mg High Risk Prophylaxis Folic Acid USP/BP 5 mg Therapeutic / Anemia Treatment Excipients Q.S. Lactose (Filler) / Starch Folic Acid, Niacinamide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Sugar Coated Tablets (typically Yellow or White). The coating protects the photosensitive vitamins from degradation.
Active Ingredient Strength (Standard) Therapeutic Role Folic Acid USP/BP 1.5 mg / 5 mg DNA Repair / Anemia Prevention Niacinamide USP/BP 20 mg / 50 mg / 100 mg Metabolic Support / Skin Barrier Excipients Q.S. Dibasic Calcium Phosphate / Starch Filler / Disintegrant Fortified Procaine Peniciilin Injection with Streptomycin
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Strength Role Procaine Penicillin G 300,000 IU Sustained Release (24 Hours) Benzyl Penicillin Sodium 100,000 IU Rapid Onset (Peak Levels) Streptomycin Sulfate Equivalent to 0.5 g (500 mg) Base Gram-Negative Coverage Total Formulation 400,000 IU + 0.5 g Standard Adult Dose *Pack Sizes: Tray of 50 Vials or 100 Vials.
Fortified Procaine Penicillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials.
Active Ingredient Proportion Role Procaine Penicillin G 300,000 IU (75%) Long Acting (Depot) Benzyl Penicillin Sodium 100,000 IU (25%) Rapid Acting (Peak) Total Strength 400,000 IU (4 Lac) Standard Adult Dose Total Strength 4,000,000 IU (40 Lac) High Dose / Veterinary *Pack Sizes: Tray of 50 Vials or 100 Vials.
FRUSEMIDE INJECTION
FreeComposition
Each ml. contains: Frusemide I.P. ……..……….. 10 mg.
Benzyl Alcohol I.P. ………….1.0 % w/v
(As Preserva9ve )
Water for Injec9on I.P ……….. Q.S 2 mlUsage: – High blood pressure, heart failure and edema
Category: – Diuretic injection
Therapeutic category: – Diuretic
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
Frusemide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Light Sensitive). We offer a wide range of strengths, including high-dose variants for renal failure.
Active Ingredient Strength (Standard) Primary Indication Frusemide USP/BP/IP 20 mg Geriatric / Mild Edema Frusemide USP/BP/IP 40 mg Standard Adult Dose Frusemide USP/BP/IP 500 mg Severe Renal Failure (Dialysis Support) Excipients Q.S. Lactose / Starch / Talc Frusemide veterinary injection
FreeComposition
Frusemide VET INJ. 10ML
Usage: –It is crucial to follow the veterinarian’s prescription and dosage instructions precisely.
Category: – veterinary practice
Therapeutic category: – veterinary practice
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
Fulvestrant Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Oily Solution in Prefilled Syringes (PFS) or Vials. (Note: This is a high-viscosity injection).
Active Ingredient Strength Volume Fulvestrant USP/BP 250 mg 5 ml Prefilled Syringe (50 mg/ml) Fulvestrant USP/BP 250 mg 5 ml Vial (50 mg/ml) Vehicle Castor Oil / Benzyl Alcohol Viscous Oily Base *Pack Sizes: Box of 1 PFS (with safety needles) or Box of 2 PFS (for 500mg dose).
Furazolidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Light-Shielded Tablet, packed exclusively in highly secure, opaque Alu-PVC or heavy-gauge Alu-Alu blister strips to ensure the absolute chemical survival of the intensely photolabile (light-sensitive) nitrofuran molecule.
Active Ingredient Strength Primary Clinical Function Furazolidone USP/Ph.Eur. 100 mg Global Outbreak & Dysentery Standard: The definitive therapeutic unit utilized for rapid, massive-dose eradication of intestinal protozoa and severe bacterial enteritis. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Premium Opacifying Film-Coat Diluent / Superdisintegrant / Binder / Lubricant / UV-Barrier Film (Engineered specifically using heavy Titanium Dioxide film-coating to block ultraviolet light, preventing the yellow Furazolidone powder from oxidizing and degrading into a useless brown paste before ingestion) *Pack Sizes: 10×10 Blisters (Optimized specifically for rapid NGO deployment and short-course 5-to-7 day dysentery eradication protocols).
Furosemide & Spironolactone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Furosemide USP/Ph.Eur. 20 mg The Loop Diuretic (Fluid Clearance): Rapidly eliminates severe fluid buildup (edema) from the lungs, abdomen, and peripheral tissues. Spironolactone USP/Ph.Eur. 50 mg The Potassium-Sparing Shield: Blocks aldosterone, prevents toxic cardiac fibrosis, and heavily protects the patient against lethal hypokalemia. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Slipper-Coating (Engineered utilizing advanced wet-granulation to ensure both the rapid-acting Furosemide and the slower-acting Spironolactone dissolve at precise, synchronized rates to guarantee the electrolyte-sparing synergy) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict chronic cardiology and hepatology dispensing regimens).
Furosemide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Furosemide USP/BP 20 mg 2 ml Ampoule (10 mg/ml) – Standard Furosemide USP/BP 40 mg / 4 ml 4 ml Ampoule – High Dose Furosemide USP/BP 250 mg / 25 ml 25 ml Vial – Renal Failure Excipients Sodium Hydroxide / NaCl pH Adjuster / Isotonicity *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Gabapentin & Amitriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 300 mg / 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals. Amitriptyline (as Hydrochloride) USP/Ph.Eur. 10 mg The Synaptic Enhancer (Micro-Dose): The highly potent TCA required to amplify descending pain inhibition and restore sleep patterns. Excipients Microcrystalline Cellulose / Crospovidone / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 10mg micro-dose of Amitriptyline is flawlessly distributed throughout the massive Gabapentin matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Gabapentin & Methylcobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable FDC Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the ultra-fragile B12 molecule.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 300 mg / 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals and stop the shooting pain. Methylcobalamin (Mecobalamin) JP/USP 500 mcg / 1500 mcg The Myelin Regenerator (Micro-Dose): The highly potent, biologically active B12 analogue required to stimulate axonal growth and rebuild the damaged myelin sheath. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Titanium-Dioxide Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered utilizing strictly segregated blending or Bilayer technology to prevent the massive Gabapentin dose from degrading the microscopic Methylcobalamin, finished with a heavy, opaque film-coat to act as an absolute UV/Light barrier) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic diabetic and neurology dispensing regimens).
Gabapentin & Nortriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals. Nortriptyline (as Hydrochloride) USP/Ph.Eur. 10 mg The Synaptic Enhancer (Micro-Dose): The highly potent TCA required to amplify descending pain inhibition and restore sleep patterns. Excipients Microcrystalline Cellulose / Crospovidone / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 10mg micro-dose of Nortriptyline is flawlessly distributed throughout the massive 400mg Gabapentin matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Gabapentin Capsules
FreeGabapentin capsules (commonly 100 mg, 300 mg, and 400 mg) contain the active pharmaceutical ingredient gabapentin USP, along with a variety of inactive excipients that aid in the drug’s delivery and stability.
Gabapentine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the heavily compressed active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 600 mg Global Neuropathy Standard: The definitive high-dose unit utilized for the aggressive, long-term maintenance of severe diabetic peripheral neuropathy and postherpetic neuralgia. Gabapentin USP/Ph.Eur. 800 mg Max-Dose Seizure & Refractory Pain Standard: Massive therapeutic payload utilized for high-dose titration (up to 3600 mg/day) in refractory partial-onset seizures and extreme nerve pain. Excipients Copovidone / Crospovidone / Microcrystalline Cellulose / Magnesium Stearate / Premium Polymeric Film High-Shear Binder / Superdisintegrant / Diluent / Slipper-Coating (Engineered specifically utilizing advanced wet-granulation to compress the massive, fluffy 800mg API into a dense, smooth, swallowable tablet, preventing the pill from becoming a dangerous choking hazard for elderly patients) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for chronic, high-volume daily dispensing regimens).
Ganciclovir Capsules
FreeGanciclovir capsules (commonly found in 250 mg and 500 mg strengths) contain the active antiviral drug ganciclovir, a synthetic guanine derivative used to treat and prevent cytomegalovirus (CMV) infections
Ganciclovir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the active pharmaceutical ingredient and protect healthcare handlers from cytotoxic exposure.
Active Ingredient Strength Primary Clinical Function Ganciclovir USP/Ph.Eur. 250 mg Renal Titration Standard: Base therapeutic unit utilized for strict, calculated dose reductions in transplant patients suffering from severe renal impairment (low creatinine clearance). Ganciclovir USP/Ph.Eur. 500 mg Global Maintenance Standard: High-efficacy adult maintenance dose utilized for daily, long-term suppression of CMV retinitis to prevent viral relapse. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant / Heavy Film-Coating (Engineered specifically to lock the highly mutagenic and carcinogenic API safely inside the tablet, completely preventing caregiver and pharmacist exposure to toxic airborne dust) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 84 (Optimized specifically for strict, high-volume chronic infectious disease dispensing regimens).
Gefitinib tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the targeted antineoplastic agent.
Active Ingredient Strength Primary Clinical Function Gefitinib USP/Ph.Eur. 250 mg Global Adult Oncology Standard: The definitive, highly precise daily maintenance dose required to maintain constant, paralyzing pressure on the mutated EGFR protein to keep the lung cancer in deep molecular remission. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Sodium Lauryl Sulfate / Magnesium Stearate / Premium Polymeric Film Diluent / Binder / Superdisintegrant / Surfactant / Heavy Film-Coating (Engineered specifically to maximize the dissolution of this poorly soluble compound while locking the cytotoxic API safely inside the tablet, completely preventing handler and pharmacist exposure to the carcinogenic dust) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Gemcitabine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Gemcitabine Hydrochloride USP/BP Equivalent to 200 mg Gemcitabine Low Dose / Adjustment Gemcitabine Hydrochloride USP/BP Equivalent to 1000 mg (1 g) Standard Adult Dose Gemcitabine Hydrochloride USP/BP Equivalent to 1400 mg (1.4 g) High Dose / Large BSA Excipients Mannitol / Sodium Acetate Bulking Agent / Buffer *Pack Sizes: Tray of 1 Vial. (Cytotoxic Packaging).
Gentamicin Injection
FreeGentamicin injection (brand name Garamycin) is a sterile, clear, colourless to slightly yellow aqueous solution of an aminoglycoside antibiotic. It is used to treat serious gram-negative bacterial infections.
Gentamicin injection
FreeComposition
Each 2 ml Contains :Gentamicin Sulphate I.P.
Equiv. To. Gentamicin base 80 mg
Methyl Paraben I.P 0.18 % W/V ( As Preserva9ve )
Propyl Paraben I.P 0.02 % W/V ( As Preserva9ve )
Water for Injection I.P. Q.S. 2 ml AMP, 10 ml, 20 ml, 30 mlEach 2 ml Contains :Gentamicin Sulphate I.P.
Equi. To. Gentamicin base 20 mg
Methyl Paraben I.P 0.18 % W/V( As Preserva9ve )
Propyl Paraben I.P 0.02 % W/V( As Preserva9ve )
Water for Injec9on I.P. Q.S. 2 ml AMPsage: – It is commonly used to treat various bacterial infections
Category: – antibiotic injection
Therapeutic category: – antibiotic medication
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
Gentamicin Veterinary injection
FreeComposition
Gentamicin VET INJ. 30 M
Gentamicin VET INJ. 100 ML
Usage: – It is commonly used to treat various bacterial infections Animal
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
Ginkgo Biloba Extract ,Piracetam & Vinpocetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the combined phyto-synthetic payloads.
Active Ingredient Strength Primary Clinical Function Piracetam USP/Ph.Eur. 400 mg / 800 mg The Nootropic Anchor: Massive synthetic payload required to force neuroplasticity, enhance membrane fluidity, and restore memory function in damaged neural networks. Ginkgo Biloba Extract (Standardized) 60 mg The Microcirculatory Botanical: Standardized extract to prevent capillary clotting and shield the brain from oxidative stress. Vinpocetine USP/Ph.Eur. 5 mg The Cerebral Oxygenator (Micro-Dose): Targeted vasodilation of cerebral arteries to immediately restore oxygen delivery to ischemic tissues. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Polyvinylpyrrolidone (PVP) / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Binder / Slipper-Coating (Engineered specifically to compress the incredibly bulky Piracetam alongside the sticky herbal extract into a single, dense, swallowable pill, heavily coated to lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic 3-to-6 month neurology dispensing regimens).
Ginkgo Biloba Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Pharmaceutical-Grade Botanical Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic herbal extract.
Active Ingredient Strength Primary Clinical Function Standardized Ginkgo Biloba Extract (Leaves) 40 mg The Tinnitus & Vertigo Standard: Base therapeutic unit frequently prescribed three times daily for the management of inner-ear microcirculatory disorders (tinnitus and dizziness). Standardized Ginkgo Biloba Extract (Leaves)
*Strictly Standardized to 24% Ginkgo Flavone Glycosides & 6% Terpene Lactones (EGb 761 Equivalent)80 mg / 120 mg The Cognitive & Vascular Standard: High-efficacy adult macro-doses utilized for the targeted treatment of vascular dementia, Alzheimer’s disease adjunct therapy, and intermittent claudication. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Anhydrous Silica / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Lubricant (Engineered utilizing strictly climate-controlled dry-granulation to prevent the intensely sticky botanical extract from agglomerating, heavily coated to lock out humidity and prevent the characteristic pungent botanical odor) *Pack Sizes: 10×10 Blisters or Bottles of 60 (Optimized specifically for chronic, lifelong neuro-vascular maintenance).
Glibenclamide & Metformin Hydrochloride Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) designed for flexible clinical titration.
Active Ingredient Standard Strengths (per Tablet) Primary Clinical Function Metformin HCl 400 mg / 500 mg The Foundation: Reduces glucose production. Glibenclamide (Glyburide) 2.5 mg / 5 mg The Stimulator: Enhances insulin secretion. Excipients Pharma Grade The Matrix: Ensures stability of the FDC. Glibenclamide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The tablet is usually white or pink and scored to allow for precise dose titration.
Active Ingredient Strength (Standard) Role Glibenclamide USP/BP 1.25 mg Geriatric / Renal Impairment Glibenclamide USP/BP 2.5 mg Initial Dose / Mild Diabetes Glibenclamide USP/BP 5 mg Standard Therapeutic Dose Excipients Q.S. Lactose (Diluent) / Maize Starch Glibenclamide, Metformin & Pioglitazone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the three highly reactive APIs.
Active Ingredient Strength Primary Clinical Function Glibenclamide USP/Ph.Eur. 5 mg The Secretagogue (Micro-Dose): Triggers rapid, potent insulin release from the pancreas to control acute post-prandial (after-meal) glucose spikes. Pioglitazone (as Hydrochloride) USP/Ph.Eur. 15 mg The Sensitizer (Micro-Dose): Reverses deep cellular insulin resistance in skeletal muscle and adipose tissue. Metformin Hydrochloride USP/Ph.Eur. 500 mg (IR or ER) The Hepatic Anchor (Macro-Dose): Provides baseline suppression of liver glucose production. Frequently formulated in a sustained-release matrix to minimize severe GI side effects. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Hypromellose / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder (ER Polymer) / Lubricant (Engineered utilizing elite multi-stage geometric dilution to guarantee that the lethal 5mg micro-dose of Glibenclamide is flawlessly and evenly distributed throughout the massive 500mg Metformin matrix) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic diabetic dispensing regimens).
Gliclazide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Immediate Release) or Modified Release (MR) Tablets (Once Daily).
Active Ingredient Strength Formulation Role Gliclazide BP/EP 80 mg Immediate Release Standard Divided Dose Gliclazide BP/EP 30 mg Modified Release (MR) Once Daily (Start) Gliclazide BP/EP 60 mg Modified Release (MR) Once Daily (Maintenance) Excipients Q.S. HPMC (Matrix) / Lactose Release Control Glimepiride & Metformin Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Bilayered Tablets or Film Coated Tablets. The bilayered technology is often used to manage the different release profiles and physical characteristics of the two APIs.
Active Ingredient Strength (Standard) Therapeutic Role Glimepiride USP/BP/IP 1 mg / 2 mg Sulfonylurea (Insulin Secretagogue) Metformin HCl USP/BP/IP 500 mg / 1000 mg Biguanide (Insulin Sensitizer) Excipients Q.S. Povidone / Magnesium Stearate Stabilizing Core Matrix Glimepiride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (often color-coded by strength). This allows for precise titration from very low doses.
Active Ingredient Strength (Standard) Color Code (Typical) Role Glimepiride USP/BP/IP 1 mg Pink Initial Dose Glimepiride USP/BP/IP 2 mg Green Titration Step 1 Glimepiride USP/BP/IP 3 mg Yellow Titration Step 2 Glimepiride USP/BP/IP 4 mg Blue Maintenance / High Dose Glimepiride, Pioglitazone & Metformin Hydrochloride Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) designed for flexible clinical titration.
Active Ingredient Common Strength Primary Clinical Function Metformin HCl (SR/IR) 500 mg / 1000 mg The Foundation: Reduces glucose production. Glimepiride 1 mg / 2 mg The Stimulator: Enhances insulin secretion. Pioglitazone 15 mg The Sensitizer: Fixes insulin resistance. Glipizide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Immediate Release) or Extended Release (XL/SR) Tablets using osmotic pump or matrix technology.
Active Ingredient Strength Formulation Role Glipizide USP/BP 5 mg Immediate Release Standard Initial Dose Glipizide USP/BP 10 mg Immediate Release High Potency Maintenance Glipizide USP/BP 5 mg / 10 mg Extended Release (XL) Once Daily (24hr Control) Excipients Q.S. Lactose / Stearic Acid Binder / Lubricant Glucosamine ,Chondroitin & Diacerein Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Oblong Caplet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic sulfate salts.
Active Ingredient Strength Primary Clinical Function Glucosamine Sulfate Potassium Chloride USP/Ph.Eur. 750 mg The Structural Foundation: Massive therapeutic payload required to stimulate raw cartilage synthesis. Chondroitin Sulfate Sodium USP/Ph.Eur. 200 mg / 250 mg The Hydraulic Restorer: Pulls water into the joint matrix to restore physical shock-absorption and elasticity. Diacerein USP/Ph.Eur. 50 mg The Biochemical Brake: Direct Interleukin-1 (IL-1) inhibition to halt the enzymatic degradation of the joint space. Excipients Microcrystalline Cellulose / Povidone K-30 / Croscarmellose Sodium / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / High-Shear Binder / Superdisintegrant / Lubricant / Slipper-Coating (Engineered specifically to compress over 1000mg of bulky, powdery API into a single, dense, swallowable “caplet” without crumbling, heavily coated to mask the bitter taste and lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic orthopedic dispensing regimens).
Glucosamine Capsule
FreeGlucosamine capsules typically contain one or more forms of glucosamine, an amino sugar essential for building cartilage and joint tissues. These active ingredients are often derived from the shells of shellfish (crabs, shrimp, and lobsters) or produced from vegetarian sources like fermented corn or fungi.
Glucosamine Sulphate Chondroitin Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Large Oval/Caplet shape). The formulation is optimized for high bioavailability and stability.
Active Ingredient Strength Source/Form Glucosamine Sulphate
(as Glucosamine Sulphate Potassium Chloride)500 mg Marine (Shellfish) Exoskeletons Chondroitin Sulphate Sodium 400 mg Bovine / Shark Cartilage (High Purity) Excipients Q.S. PVP K-30 (Binder) / Titanium Dioxide Glucose Infusion 10%
FreeActive IngredientStrength (per 100 ml)Primary Clinical FunctionGlucose (Dextrose) IP/BP/USP10.0 gThe Fuel: Provides 34 kcal per 100 ml.ExcipientsWater for Injection (WFI)The Vehicle: Sterile and pyrogen-free.Osmolarity~505 mOsm/LThe Physics: Hypertonic solution.pH Range3.5 to 6.5The Stability: Chemically optimized for shelf-life.
Glyceryl Trinitrate Tablets
FreeProduct Composition & Strength
We supply this product as Sublingual Tablets (Dissolve under tongue) or Sustained Release (SR) Tablets (Swallow whole for prevention).
Active Ingredient Strength Formulation Role Diluted Glyceryl Trinitrate USP 0.5 mg (500 mcg) Sublingual (SL) Acute Attack Rescue Diluted Glyceryl Trinitrate USP 2.6 mg Sustained Release (SR) Angina Prophylaxis Diluted Glyceryl Trinitrate USP 6.4 mg Sustained Release (SR) High Dose Maintenance Excipients Q.S. Lactose (Adsorbent) / Stearates Stability Matrixt Griseofulvin Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). Critical to its efficacy is the particle size; we strictly use Micronized API to ensure adequate absorption.
Active Ingredient Strength (Standard) Form Role Griseofulvin USP/BP 125 mg Micronized Pediatric (Tinea Capitis) Griseofulvin USP/BP 250 mg Micronized Standard Adult Dose Griseofulvin USP/BP 500 mg Micronized High Dose / Resistant Cases Excipients Q.S. Povidone / Maize Starch Binder / Disintegrant Haematinic Capsules
FreeHaematinic capsules are combination supplements containing essential nutrients required for the production of healthy red blood cells and haemoglobin. While specific formulations vary by brand, they typically contain the following categories of ingredients:
Haloperidol Injection
FreeComposition
Each ml Contains :Haloperidol I.P. …………… 5 mg
Methyl Paraben I.P 0.18 % W/V( As Preserva9ve )
Propyl Paraben I.P 0.02 % W/V( As Preserva9ve )
Water for Injec9on I.P. Q.S. 1mlUsage: – Treat certain mental/mood disorders
Category: – Antipsychotic / CNS injection
Therapeutic category: –Haloperidol Injection
Haloperidol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (often small, white or yellow). We offer a wide range of strengths for precise titration.
Active Ingredient Strength (Standard) Primary Role Haloperidol USP/BP 1.5 mg Geriatric / Maintenance Haloperidol USP/BP 5 mg Standard Acute Dose Haloperidol USP/BP 10 mg Severe Psychosis / Mania Haloperidol USP/BP 20 mg Treatment Resistant Cases Heparin Sodium Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Vials.
Active Ingredient Strength Volume Heparin Sodium USP/BP 5,000 IU (1,000 IU/ml) 5 ml Multi-Dose Vial Heparin Sodium USP/BP 25,000 IU (5,000 IU/ml) 5 ml Multi-Dose Vial Preservative Benzyl Alcohol 0.95% v/v *Available in preservative-free versions for neonatal use upon request.
HP Kit (Pantoprazole,Metronidazole & Clarithromycin Tablets)
FreeProduct Composition & Strength
We supply this product as a Precision-Packed, Multi-Component Combi-Kit, packed exclusively in highly secure, day-labeled Alu-Alu blister strips to ensure the absolute chemical stability of all three distinct APIs while forcing flawless patient compliance.
Active Component (Per Daily Blister) Strength & Form Primary Clinical Function Pantoprazole Sodium USP/Ph.Eur.
(2 Tablets per kit)40 mg (Gastro-Resistant / Enteric Coated) The Environmental Modulator: Suppresses acid, heals the ulcer, and creates the required pH for antibiotic survival. (Must be heavily enteric-coated to survive the stomach and absorb in the duodenum). Clarithromycin USP/Ph.Eur.
(2 Tablets per kit)500 mg (Film-Coated) The Primary Bacteriostatic: Halts bacterial protein synthesis. Heavy film-coating masks the intensely bitter, metallic macrolide taste. Metronidazole USP/Ph.Eur.
(2 Tablets per kit)400 mg / 500 mg (Film-Coated) The Bactericidal Finisher: Destroys bacterial DNA. Crucial alternative to Amoxicillin for penicillin-allergic demographics or regions with high amoxicillin resistance. *Pack Sizes: 1 Day Kit (containing 6 tablets total: 1 of each for Morning, 1 of each for Evening). Generally supplied in 7-Day or 14-Day Full Therapy Cartons.
Hucog
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection accompanied by a solvent (Sodium Chloride Injection).
Brand Reference Strength Primary Use Hucog / Corion 2000 IU Pediatric Cryptorchidism / Male Fertility Hucog / Corion 5000 IU Standard Ovulation Trigger Hucog / Corion 10000 IU IVF / Assisted Reproductive Technology (ART) Solvent 0.9% NaCl 1 ml or 2 ml Ampoule *Pack Sizes: Single Vial with Ampoule or Tray of 10.
Human Albumin Injection
FreeProduct Composition & Strength
We supply this product as a Ready-to-Use Infusion in glass bottles.
Strength Volume Primary Indication Human Albumin 5% (Iso-oncotic) 250 ml / 500 ml Hypovolemic Shock / Large Burns Human Albumin 20% (Hyper-oncotic) 50 ml / 100 ml Cirrhosis / Ascites / Nephrotic Syndrome Human Albumin 25% (Hyper-oncotic) 50 ml / 100 ml Severe Hypoproteinemia / ICU Support *Stabilizers: Sodium Caprylate and Sodium Acetyltryptophanate (to prevent protein denaturation).
Hydralazine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (often Yellow or Orange). Uncoated tablets are avoided due to stability issues.
Active Ingredient Strength (Standard) Role Hydralazine HCl USP/BP 25 mg Initial Dose / Titration Hydralazine HCl USP/BP 50 mg Maintenance Dose Excipients Q.S. Coating Agents / Stabilizers Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration). Accurate low-dose titration is critical for modern therapy.
Active Ingredient Strength (Standard) Role Hydrochlorothiazide USP/BP 12.5 mg Initial Dose / Combination Use Hydrochlorothiazide USP/BP 25 mg Standard Therapeutic Dose Hydrochlorothiazide USP/BP 50 mg Edema / High Potency Excipients Q.S. Lactose (Filler) / Starch Hydrocortisone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Hydrocortisone Sodium Succinate USP/BP Equivalent to 100 mg Hydrocortisone Standard Adult / Pediatric Emergency Hydrocortisone Sodium Succinate USP/BP Equivalent to 250 mg Severe Asthma / Sepsis Pulse Hydrocortisone Sodium Succinate USP/BP Equivalent to 500 mg High-Dose ICU Protocol Excipients Sodium Phosphate / Sodium Hydroxide Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial + 1 Ampoule (WFI), 10 Vials, or 50 Vials.
Product Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Primary Use Hydrocortisone Sodium Succinate USP/BP Equivalent to 100 mg Hydrocortisone Standard Adult / Pediatric Emergency Hydrocortisone Sodium Succinate USP/BP Equivalent to 250 mg Severe Asthma / Sepsis Pulse Hydrocortisone Sodium Succinate USP/BP Equivalent to 500 mg High-Dose ICU Protocol Excipients Sodium Phosphate / Sodium Hydroxide Buffer / pH Adjuster *Pack Sizes: Tray of 1 Vial + 1 Ampoule (WFI), 10 Vials, or 50 Vials.
Hydrocortisone injection
FreeComposition
Hydrocortisone Sodium 100mg vial+wfi
Usage: – used to treat a variety of medical conditions.
Category: –Allergic injection
Therapeutic category: – Allergic Reactions
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
Hydrocortisone Oromucosal Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Mucoadhesive Pellet/Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the highly hygroscopic polymers do not prematurely swell from atmospheric humidity.
Active Ingredient Strength Primary Clinical Function Hydrocortisone (as Sodium Succinate or Acetate) USP/Ph.Eur. 2.5 mg Global Oral Pathology Standard: The definitive micro-dose engineered specifically for localized mucosal absorption, maximizing ulcer healing while neutralizing systemic exposure. Excipients Carbomer / Hypromellose (HPMC) / Lactose Monohydrate / Polycarbophil / Magnesium Stearate Bio-Adhesive Polymers / Matrix Former / Diluent / Lubricant (Engineered utilizing elite hydrophilic polymers that instantly cross-link upon contact with saliva, converting the hard tablet into an immovable, slow-release mucosal patch) *Pack Sizes: 10×10 Alu-Alu Blisters or Tubes of 20 (Optimized specifically for the short-term, acute treatment of cyclical ulcer outbreaks).
Hydrocortisone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Scored Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the micronized steroid payload.
Active Ingredient Strength Primary Clinical Function Hydrocortisone USP/Ph.Eur. 5 mg / 10 mg (Scored) Titration & Afternoon Standard: Highly precise, low-dose units engineered for pediatric CAH dosing and the critical “afternoon taper” in adult replacement therapy. Hydrocortisone USP/Ph.Eur. 20 mg (Scored) Morning Surge & Acute Flare Standard: High-efficacy dosing to replicate the natural morning cortisol spike, or for short-term suppression of acute severe allergic or inflammatory conditions. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Magnesium Stearate Diluent / Binder / Superdisintegrant / Lubricant (Engineered utilizing Micronized API—the steroid particles are milled to a microscopic size before blending to guarantee immediate, consistent gastric absorption, which is critical to avoid unpredictable hormone spikes) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict chronic, lifelong endocrinology dispensing regimens).
Hydroxy Chloroquine Sulfate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Heavy-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the photolabile active ingredient.
Active Ingredient Strength Primary Clinical Function Hydroxychloroquine Sulfate USP/Ph.Eur. 200 mg Global Rheumatology Standard: Base therapeutic unit for daily chronic maintenance in SLE and RA, allowing for exact mg/kg dosing based on ideal body weight to prevent toxicity. Excipients Dibasic Calcium Phosphate / Pregelatinized Starch / Magnesium Stearate / Polyethylene Glycol / Premium Titanium Dioxide Opadry Film Diluent / Binder / Lubricant / Heavy Opacifying Film-Coating (Engineered specifically to form an impenetrable light barrier against UV degradation, while completely masking the intensely bitter taste of the sulfate salt to ensure long-term patient compliance) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict 3-to-6 month chronic rheumatology dispensing regimens).
Hydroxy Progesterone Caproate veterinary injection
FreeComposition
Hydroxy Progesterone Caproate INJ. 2 ML
Hydroxy Progesterone Caproate INJ. 3 ML
Usage: – used to synchronize estrus (heat) cycles in female animals
Category: – veterinary medicine
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
Hydroxyurea Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Scored Film-Coated Tablet, packed exclusively in highly secure, handler-protective Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure absolute chemical stability and prevent accidental cytotoxic exposure.
Active Ingredient Strength Primary Clinical Function Hydroxyurea USP/Ph.Eur. 200 mg / 300 mg / 400 mg Pediatric Sickle Cell Standard: Specialized weight-based units designed for exact mg/kg titration in infants and children suffering from severe vaso-occlusive crises. Hydroxyurea USP/Ph.Eur. 500 mg (Scored) Global Adult Hematology Standard: High-efficacy adult maintenance dose for CML, Polycythemia Vera, and adult Sickle Cell Disease. Excipients Microcrystalline Cellulose / Sodium Citrate / Crospovidone / Magnesium Stearate / Premium Polymeric Film Diluent / pH Stabilizer / Superdisintegrant / Slipper-Coating (Engineered specifically with a heavy, durable film-coat to completely seal the highly toxic, mutagenic core away from nurses, parents, and pharmacists) *Pack Sizes: Bottles of 100 or 10×10 Alu-Alu Blisters (Optimized specifically for massive-volume NGO procurement and chronic lifetime dispensing).
Hyoscine Butylbromide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules.
Active Ingredient Strength Volume Hyoscine Butylbromide USP/BP 20 mg 1 ml Ampoule (Standard Dose) Excipients Sodium Chloride / Water for Injection Isotonic Solution *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 100 Ampoules.
Hyoscine Butylbromide Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets or Film Coated Tablets. The coating is essential to mask the naturally bitter taste of the active ingredient and ensure patient compliance.
Active Ingredient Strength (Standard) Therapeutic Role Hyoscine Butylbromide BP/USP 10 mg Muscarinic Antagonist (Antispasmodic) Excipients Q.S. Calcium Hydrogen Phosphate / Maize Starch Stabilizing Core Matrix Coating Agent Q.S. Sucrose / Talc / Acacia Traditional Sugar Coating Ibuprofen & Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The coating protects the gastric mucosa from direct contact with Ibuprofen and masks the bitter taste of the active ingredients.
Active Ingredient Strength (Standard) Therapeutic Role Ibuprofen BP/USP 200 mg NSAID (Anti-inflammatory/Analgesic) Paracetamol BP/USP 325 mg Analgesic & Antipyretic Excipients Q.S. Starch / Croscarmellose Sodium Disintegrant & Binder Ibuprofen Solution For Infusion
FreeProduct Composition & Strength
We supply this product in two formats: Ready-to-Use Infusion and Concentrate for Dilution.
Active Ingredient Strength Format Ibuprofen (with Arginine) 400 mg / 100 ml Ready-to-Use (IV Bag/Bottle) Ibuprofen (with Arginine) 400 mg / 4 ml Concentrate (Vial – Must Dilute) Solubilizer L-Arginine Ensures Water Solubility *Pack Sizes: 100 ml Bottle (Single) or Tray of 10 Vials.
Ibuprofen Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated (Round/Pink) or Film Coated Tablets. Effective taste-masking is critical as Ibuprofen has a burning aftertaste.
Active Ingredient Strength (Standard) Role Ibuprofen IP/BP/USP 200 mg OTC Standard / Fever Ibuprofen IP/BP/USP 400 mg Prescription Strength / Dental Pain Ibuprofen IP/BP/USP 600 mg Rheumatoid Arthritis (High Dose) Ibuprofen IP/BP/USP 800 mg Severe Osteoarthritis / Acute Injury Ibuprofen with Paracetamol Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) designed for maximum therapeutic synergy and patient safety.
Active Ingredient Standard Strengths (per Tablet) Primary Clinical Function Ibuprofen IP/BP/USP 200 mg / 400 mg The Anti-Inflammatory: Reduces physical swelling. Paracetamol IP/BP/USP 325 mg / 500 mg The Analgesic: Raises the chemical pain threshold. Excipients Pharma Grade The Matrix: Ensures stability and rapid release. Imatinib Capsules
FreeImatinib capsules contain the active oncology drug and a specific set of inactive ingredients designed to stabilize the compound for oral delivery.
Imatinib Mesylate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the mesylate salt.
Active Ingredient Strength Primary Clinical Function Imatinib (as Mesylate) USP/Ph.Eur. 100 mg Pediatric & Titration Standard: Base therapeutic unit utilized for weight-based pediatric leukemia dosing, or for highly precise adult dose adjustments during acute hematological toxicity. Imatinib (as Mesylate) USP/Ph.Eur. 400 mg Global Adult Oncology Standard: High-efficacy adult maintenance dose, typically taken once daily for the chronic phase of CML, or twice daily for accelerated phases and GIST. Excipients Microcrystalline Cellulose / Crospovidone / Hypromellose / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Iron-Oxide Film Diluent / Superdisintegrant / Binder / Glidant / Heavy Film-Coating (Engineered specifically to lock the cytotoxic API safely inside the tablet, completely preventing handler and pharmacist exposure to the carcinogenic dust) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Imidapril Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for precise titration). The standard strengths are optimized for maintenance therapy.
Active Ingredient Strength (Standard) Role Imidapril HCl 5 mg Initial Dose / Renal Impairment Imidapril HCl 10 mg Standard Maintenance Dose Excipients Q.S. Lactose / Macrogol Imipenem & Cilastatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Buffered Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Role Imipenem USP/BP 500 mg Antibiotic (Carbapenem) Cilastatin Sodium USP/BP Equivalent to 500 mg Cilastatin DHP-I Inhibitor Buffer Sodium Bicarbonate pH Stabilizer *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Imipramine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (often Red or Blue) to effectively mask the intensely bitter and numbing taste of the API.
Active Ingredient Strength (Standard) Primary Role Imipramine HCl USP/BP 25 mg Pediatric Enuresis / Initial Dose Imipramine HCl USP/BP 50 mg Adult Maintenance Imipramine HCl USP/BP 75 mg High Potency (Hospital Use) Excipients Q.S. Sucrose / Talc (Coating) Indapamide Tablets
FreeProduct Composition & Strength
We supply this product as Sugar/Film Coated Tablets (Immediate Release) or Sustained Release (SR) Tablets.
Active Ingredient Strength Formulation Role Indapamide USP/BP 1.5 mg Sustained Release (SR) Modern Standard Dose (24hr Control) Indapamide USP/BP 2.5 mg Immediate Release Classic Maintenance Dose Excipients Q.S. HPMC (Matrix) / Lactose Release Control Indinavir sulphate Capsules
FreeIndinavir sulphate capsules contain the active antiviral drug and several inactive ingredients used to stabilize the medication for the treatment of HIV-1 infection.
Indomethacin Capsules
FreeIndomethacin capsules contain the active nonsteroidal anti-inflammatory drug (NSAID) and a few standard pharmaceutical fillers to ensure the medication is delivered effectively
Indomethacin Tablets
FreeProduct Composition & Strength
We supply this product as Hard Gelatin Capsules (Standard) or Sustained Release (SR) Tablets.
Active Ingredient Strength (Standard) Form Role Indomethacin USP/BP 25 mg Capsule Standard Adult Dose Indomethacin USP/BP 50 mg Capsule Acute Gout / Severe Pain Indomethacin USP/BP 75 mg SR Capsule / Tablet Once/Twice Daily (Maintenance) Iron Folic Acid Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Red/Brown) or Film Coated Tablets. Sugar coating is traditional to mask the strong metallic taste of iron.
Iron Salt Salt Strength Elemental Iron Folic Acid Primary Use Dried Ferrous Sulphate 200 mg ~65 mg 0.4 mg / 400 mcg Standard Adult Prophylaxis Dried Ferrous Sulphate 200 mg ~65 mg 1 mg / 5 mg Therapeutic (Pregnancy) Ferrous Fumarate 200 mg ~65 mg 0.4 mg / 1.5 mg Sensitive Stomach / Maternal Ferrous Fumarate 300 mg ~100 mg 5 mg Severe Anemia Treatment Iron Sucrose Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dark Brown Solution in Glass Ampoules.
Active Ingredient Strength Elemental Iron Iron Sucrose Complex USP/BP 100 mg / 5 ml 20 mg/ml Iron Sucrose Complex USP/BP 50 mg / 2.5 ml 20 mg/ml pH Range 10.5 – 11.0 Highly Alkaline (Stable) *Pack Sizes: Tray of 5 Ampoules or 10 Ampoules.
Isoniazid & Pyridoxine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The ratio of Isoniazid to Pyridoxine is carefully calibrated to meet international clinical guidelines for neuroprotection.
Active Ingredient Strength (Standard) Therapeutic Role Isoniazid BP/USP 300 mg Primary Antitubercular (Bactericidal) Pyridoxine Hydrochloride BP/USP 10 mg / 25 mg / 50 mg Neuroprotective Vitamin (B6) Excipients Q.S. Starch / Lactose / Magnesium Stearate Tablet Core Matrix Isoniazid & Pyridoxine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The ratio of Isoniazid to Pyridoxine is carefully calibrated to meet international clinical guidelines for neuroprotection.
Active Ingredient Strength (Standard) Therapeutic Role Isoniazid BP/USP 300 mg Primary Antitubercular (Bactericidal) Pyridoxine Hydrochloride BP/USP 10 mg / 25 mg / 50 mg Neuroprotective Vitamin (B6) Excipients Q.S. Starch / Lactose / Magnesium Stearate Tablet Core Matrix Isoniazid Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Scored). It is often co-administered with Pyridoxine (Vitamin B6) to prevent nerve damage.
Active Ingredient Strength (Standard) Target Patient Isoniazid USP/BP/IP 100 mg Pediatric / Prophylaxis Isoniazid USP/BP/IP 300 mg Standard Adult Dose Excipients Q.S. Binder / Disintegrant Isosorbide Mononitrate Tablets
FreeProduct Composition & Strength
We supply this product as Immediate Release Tablets (20 mg). We also offer Extended Release (ER/SR) variants for once-daily dosing through our contract manufacturing division.
Active Ingredient Strength (Standard) Therapeutic Role Isosorbide Mononitrate BP/USP 20 mg Organic Nitrate / Vasodilator Excipients Q.S. Microcrystalline Cellulose / Lactose Stabilizing Matrix Isosorbide Tablets
FreeProduct Composition & Variants
We supply both Mononitrate and Dinitrate forms in immediate and sustained-release formats.
Variant Type Standard Strengths Primary Clinical Use Isosorbide Mononitrate 10mg, 20mg, 40mg Prophylaxis: Long-term prevention of angina. Isosorbide Dinitrate 5mg, 10mg, 20mg Acute & Chronic: Short and long-term heart failure. Sustained Release (SR) 30mg, 60mg Once-Daily: For improved patient compliance. Isosorbide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Oral) or Sublingual Tablets (Dissolve under tongue).
Active Ingredient Strength Route / Type Role Isosorbide Dinitrate USP/BP 5 mg Sublingual (SL)/ regular Acute Angina Attack Isosorbide Dinitrate USP/BP 10 mg Oral (Swallow) Angina Prophylaxis Isosorbide Dinitrate USP/BP 20 mg Oral (Swallow) Heart Failure / Maintenance Excipients Q.S. Lactose (Diluent) Safety / Bulk Isotretinoin Capsules
FreeProduct Composition & Strengths
We supply this product as Liquid-Filled Soft Gelatin Capsules, optimized for maximum systemic absorption.
Active Ingredient Strength (per Softgel) Primary Clinical Target Isotretinoin IP/BP/USP 10 mg Standard Starting Dose: For mild-to-moderate systemic treatment. Isotretinoin IP/BP/USP 20 mg Therapeutic Dose: For severe, cystic, or conglobate acne. Excipients Soybean Oil / Beeswax The Vehicle: Ensures lipid-solubility for better absorption. Isoxsuprine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Immediate-Release or Sustained-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Isoxsuprine Hydrochloride USP/Ph.Eur. 10 mg (IR) Acute Titration Standard: Immediate-release base unit used for the rapid initiation of therapy or carefully titrated maintenance in sensitive patients. Isoxsuprine Hydrochloride USP/Ph.Eur. 40 mg (SR) Obstetrics Maintenance Standard: High-efficacy, slow-release matrix designed specifically to provide 12-hour continuous tocolysis, vastly improving maternal compliance and protecting the cardiovascular system. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Lactose Monohydrate / Colloidal Silicon Dioxide / Magnesium Stearate ER Polymer / Diluent / Binder / Glidant / Lubricant (Engineered specifically utilizing premium Hypromellose matrices in the 40mg variant to form a robust hydrogel that slowly erodes in the gastrointestinal tract, ensuring steady-state plasma levels) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict obstetric and chronic vascular dispensing regimens).
Itopride Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Off-White) to mask the bitter taste.
Active Ingredient Strength (Standard) Role Itopride HCl 50 mg Standard Therapeutic Dose Itopride HCl 150 mg (SR) Sustained Release (Once Daily) Excipients Q.S. Lactose (Filler) / HPMC (Binder) Itraconazole Capsules
FreeItraconazole capsules contain a combination of the active antifungal drug and specialized inactive ingredients designed to overcome the medication’s poor solubility in water.
Ivabradine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Ivabradine (as Hydrochloride) USP/Ph.Eur. 5 mg Initiation / Titration Standard: Base therapeutic unit utilized twice daily for the safe initiation of therapy, allowing the cardiologist to monitor resting heart rate before upward titration. Ivabradine (as Hydrochloride) USP/Ph.Eur. 7.5 mg Global Maintenance Standard: High-efficacy adult maintenance dose to strictly maintain the resting heart rate between 50 and 60 beats per minute. Excipients Lactose Monohydrate / Maize Starch / Maltodextrin / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Glidant / Lubricant / Film-Coating (Engineered specifically using precise geometric dilution to ensure the micro-dose API is flawlessly distributed, preventing accidental bradycardia from “hot spots” in a poorly blended generic tablet) *Pack Sizes: 10×10 Blisters or Bottles of 56 (Optimized specifically for strict 28-day chronic cardiology dispensing regimens).
Ivermactin veterinary injection
FreeComposition
Ivermactin INJ. 10 ML
Ivermactin INJ. 50 ML
Usage: – It is also used to control external parasites such as mites, lice, and ticks in animals.
Category: – veterinary injection medicine
Therapeutic category: –veterinary injection 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
Ivermectin & Clorsulon veterinary INJECTION
FreeCOMPOSITION
Ivermectin 1% & Clorsulon 10% VET INJ. 10 ML
Usage: – Treat or prevent Common Veterinary Uses
Category: –Common Veterinary injection
Therapeutic category: Veterinary injection
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
Ivermectin Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Scored). The dosage is strictly weight-based.
Active Ingredient Strength (Standard) Role Ivermectin USP/BP/EP 3 mg Pediatric / Low Body Weight Ivermectin USP/BP/EP 6 mg Standard Adult Unit Ivermectin USP/BP/EP 12 mg High Strength (Adult Dose) Excipients Q.S. Microcrystalline Cellulose (Filler) Ketoconazole Tablets
FreeProduct Composition & Available Specifications
We supply Ketoconazole in the internationally recognized 200 mg therapeutic dosage configuration, engineered to optimize plasma saturation kinetics and ensure maximum cellular bioavailability.
Active Ingredient Monograph Calibrated Strength Formulation Matrix Delivery System Primary Clinical Application Ketoconazole USP / BP / IP 200 mg Oral Solid Immediate-Release Uncoated Tablet Systemic Antifungal Care: First-line systemic management of blastomycosis, coccidioidomycosis, histoplasmosis, and severe recalcitrant tinea infections. Excipients Pharma Grade Lactose Monohydrate, Corn Starch, Povidone K-30, Magnesium Stearate The Disintegration Scaffold: Calibrated matrix for high mechanical core stability and rapid wicking in gastric fluids. Ketoprofen veterinary injection
FreeComposition
Ketoprofen VET INJ. 15 ML
Ketoprofen VET INJ. 100 ML
Usage: –It is used in various animal species, including dogs, cats, horses, and livestock.
Category: – veterinary injection
Therapeutic category: –veterinary injection
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
Ketorolac Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules.
Active Ingredient Strength Volume Ketorolac Tromethamine USP/BP 30 mg 1 ml Ampoule (Standard Dose) Ketorolac Tromethamine USP/BP 60 mg 2 ml Ampoule (High Dose) Excipients Alcohol USP / Sodium Chloride Solubilizer / Isotonicity *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 50 Ampoules.
Ketorolac injection
FreeComposition
INJ (1 ML) Each ml contains –
Ketorolac Tromethamine 30 mg + WFI IP Q.S.
Usage: – Relieve moderately severe pain
Category: – Anti-inflammatory injection (NSAIDs)
Therapeutic category: – NSAIDs
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
Ketorolac Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (White/Round). The standard oral dosage is strictly limited due to potency.
Active Ingredient Strength (Standard) Role Ketorolac Tromethamine USP/BP 10 mg Standard Adult Dose Excipients Q.S. Microcrystalline Cellulose / Lactose L- ornithine-L-aspartate tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical and physical stability of the highly hygroscopic amino acid salt.
Active Ingredient Strength Primary Clinical Function L-Ornithine L-Aspartate (LOLA) 150 mg / 250 mg Hepatology Maintenance Standard: Base therapeutic units for long-term chronic management of severe Non-Alcoholic Fatty Liver Disease (NAFLD), alcoholic hepatitis, and mild hyperammonemia. L-Ornithine L-Aspartate (LOLA) 500 mg Acute Detoxification Standard: High-efficacy adult therapy utilized for immediate ammonia reduction and the step-down management of Hepatic Encephalopathy following hospital discharge. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Film-Coating (Engineered specifically to lock out atmospheric moisture, preventing the heavy 500mg amino acid tablet from swelling, cracking, or prematurely degrading before it reaches the patient’s stomach) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, high-volume chronic hepatology dispensing regimens).
L-Methylfolate Calcium ,Pyridoxal-5-Phosphate & Mecobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the three delicate coenzymes.
Active Ingredient Strength Primary Clinical Function L-Methylfolate Calcium USP/Ph.Eur. 1 mg Active Vitamin B9: Direct methyl-donor for homocysteine remethylation and massive neurotransmitter synthesis. Pyridoxal-5-Phosphate (P5P) USP/Ph.Eur. 0.5 mg Active Vitamin B6: Immediate catalyst for transsulfuration; drastically reduces the risk of paradoxical sensory neuropathy seen with cheap Pyridoxine. Mecobalamin (Methylcobalamin) USP/Ph.Eur. 1500 mcg Active Vitamin B12: Direct peripheral nerve repair, myelin synthesis, and essential co-factor for homocysteine neutralization. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / Heavy UV-Blocking Coating (Engineered specifically to form an impenetrable light barrier, completely preventing the photolabile degradation of the active B12 and folate components) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology and diabetic dispensing regimens).
L-Ornithine-L-Aspartate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Hypertonic Solution in Glass Ampoules. (Must be diluted).
Active Ingredient Strength Concentration L-Ornithine-L-Aspartate 5 g (5000 mg) 500 mg/ml (10 ml Ampoule) Excipients Water for Injection – *Pack Sizes: Tray of 5 Ampoules or 10 Ampoules.
Lactobacillus SporogenesTablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Moisture Matrix Tablet, packed exclusively in highly secure Alu-Alu blister strips or tightly sealed Alu-PVC blisters to prevent premature ambient moisture from triggering spore germination prior to ingestion.
Active Ingredient Strength Primary Clinical Function Lactobacillus sporogenes (Bacillus coagulans) Spores 60 Million Spores (CFU) Global Microbiome Standard: High-density, survival-guaranteed spore count to aggressively recolonize the intestinal lining, halt acute diarrhea, and outcompete opportunistic pathogens following heavy antibiotic therapy. Excipients Microcrystalline Cellulose / Lactose Anhydrous / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Glidant / Lubricant (Engineered specifically utilizing ultra-low moisture excipients during dry-blending to ensure the dormant spores are not accidentally “woken up” and destroyed by water activity on the factory floor) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for massive-volume retail pharmacy and pediatric clinic dispensing).
Lamivudine & Zidovudine tablets
FreeProduct Composition & Strength
We supply this product in the internationally standardized Fixed-Dose Combination (FDC) required for therapeutic compliance.
Active Ingredient Strength (per Tablet) Primary Clinical Function Lamivudine (3TC) IP/BP/USP 150 mg The Chain Terminator: High potency, low toxicity. Zidovudine (AZT) IP/BP/USP 300 mg The Foundation: Proven efficacy in preventing replication. Excipients Pharma Grade The Matrix: Ensures stability of the sensitive FDC. Lamivudine Tablets
FreeProduct Composition & Available Portfolio strengths
We manufacture Lamivudine across the precise compendial strengths mandated to manage either targeted chronic hepatic monotherapy or high-potency systemic combination antiretroviral protocols.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Lamivudine USP / BP / IP 100 mg Oral Solid Film-Coated Tablet Chronic Hepatitis B (HBV): Low-dose configuration optimized for standalone daily suppression of active hepatic viral replication. Lamivudine USP / BP / IP 150 mg Oral Solid Film-Coated Tablet Standard Antiretroviral (HIV): Baseline strength designed for twice-daily co-administration or integration into standard multi-drug ARV regimens. Lamivudine USP / BP / IP 300 mg Oral High-Potency Solid Tablet High-Compliance Antiretroviral (HIV): Standard adult once-daily high-dose format engineered to optimize long-term patient compliance. Lamivudine, Zidovudine & Nevirapine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often White or Off-White). This FDC is designed for patients who have successfully completed the Nevirapine “lead-in” phase.
Active Ingredient Strength (Standard) Class Lamivudine USP/BP 150 mg NRTI (Cytidine Analog) Zidovudine USP/BP 300 mg NRTI (Thymidine Analog) Nevirapine USP/BP 200 mg NNRTI Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Lamotrigine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet or Rapid-Dispersible (DT) Tablet, packed exclusively in highly secure Alu-PVC or Alu-Alu blister strips, frequently customized into highly regulated Titration Starter Kits.
Active Ingredient Strength Primary Clinical Function Lamotrigine USP/Ph.Eur. 25 mg (Starter Kit) The SJS-Prevention Standard: Mandatory base unit for the strict, slow titration schedule required to prevent fatal cutaneous reactions. Often formulated as a Dispersible Tablet (DT) for pediatric epilepsy. Lamotrigine USP/Ph.Eur. 50 mg / 100 mg / 200 mg Global Maintenance Standard: High-efficacy adult maintenance doses for lifelong seizure control and bipolar stabilization. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Sucralose & Flavoring (If DT) / Magnesium Stearate Diluent / Superdisintegrant / Binder / Sweetener (Engineered specifically to either swallow intact or disperse rapidly in a teaspoon of water for children or elderly psychiatric patients suffering from dysphagia) *Pack Sizes: 10×10 Blisters, Bottles of 100, or Dedicated 28-Day Titration Calendar Packs (Optimized specifically to eliminate caregiver dosing errors during the critical initiation phase).
Lamotrigine Tablets
FreeProduct Composition & Available Strengths
Because Lamotrigine demands highly delicate, low-dose introductory titration to ensure patient dermatological safety, we manufacture the full compendial strength matrix.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Lamotrigine USP / BP / IP 25 mg Oral Solid Uncoated / Dispersible Tablet Dermatological Intro Titration: Mandatory low-dose baseline format utilized exclusively for the critical initial 2-week dose-escalation phase. Lamotrigine USP / BP / IP 50 mg Oral Solid Uncoated / Dispersible Tablet Intermediate Step-Up Dosing: Step-up strength calibrated for weeks 3 and 4 of therapy to safely approach steady-state plasma metrics. Lamotrigine USP / BP / IP 100 mg Oral Solid Compressed Tablet Standard Maintenance Block: First-line international standard strength for adult maintenance monotherapy in epilepsy and bipolar stabilization. Lamotrigine USP / BP / IP 200 mg Oral High-Potency Solid Tablet Maximal Saturation Maintenance: High-strength configuration calibrated for advanced refractory partial seizures and combination therapies. Lansoprazole & Domperidone Capsules
FreeLansoprazole and Domperidone combination capsules contain two active medications used to treat symptoms of acid reflux and slow digestion. They are often formulated as multi-particulate systems (pellets or granules) within a single hard gelatin capsule to ensure stable delivery.
Lansoprazole Capsules
FreeLansoprazole capsules are composed of an active drug and various inactive ingredients (excipients) that ensure the medication is released properly in the body.
Lansoprazole Dispersible Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, MUPS-Based Dispersible Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical survival of the delicate, moisture-sensitive micro-pellets.
Active Ingredient Strength Primary Clinical Function Lansoprazole (as Enteric-Coated Micro-Pellets) USP/Ph.Eur. 15 mg Maintenance & Pediatric Standard: Base therapeutic unit for healing maintenance, pediatric GERD, and preventing NSAID-induced gastric ulcers. Lansoprazole (as Enteric-Coated Micro-Pellets) USP/Ph.Eur. 30 mg Acute Healing Standard: High-efficacy adult dosing for the rapid healing of erosive esophagitis, active duodenal ulcers, and H. pylori eradication protocols. Excipients Methacrylic Acid Copolymer (Enteric Coat) / Crospovidone / Microcrystalline Cellulose / Mannitol / Sucralose / Strawberry Flavor Acid-Resistant Shield / Superdisintegrant / Diluent / Sweetener (Engineered specifically to create a highly palatable, rapid-burst suspension that masks the bitter API, ensuring high pediatric compliance and smooth NG tube transit) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, highly monitored hospital and outpatient dispensing regimens).
Lansoprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Form Lansoprazole Sodium USP/BP Equivalent to 30 mg Lansoprazole White Lyophilized Cake Excipients Mannitol / Meglumine / Sodium Hydroxide Bulking Agent / pH Stabilizer *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials.
Ledipasvir & Sofosbuvir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dual-Active FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles with specialized desiccants to ensure the absolute chemical survival of the complex antiviral APIs.
Active Ingredient Strength Primary Clinical Function Ledipasvir USP/Ph.Eur. 90 mg The NS5A Anchor: Potent inhibitor of viral assembly and secretion; highly effective against specific HCV genotypes. Sofosbuvir USP/Ph.Eur. 400 mg The NS5B Backbone: The globally recognized foundational DAA that forces viral RNA chain termination across multiple genotypes. Excipients Copovidone / Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Binder / Diluent / Superdisintegrant / Lubricant / Film-Coating (Engineered specifically to solve the massive solubility differences between the highly soluble Sofosbuvir and the poorly soluble Ledipasvir, guaranteeing synchronized gastric release and peak systemic absorption) *Pack Sizes: Bottles of 28 (Optimized specifically for the strict 4-week dispensing intervals required for 8, 12, or 24-week curative regimens).
Ledipasvir Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Solid-Dispersion Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical survival of the complex antiviral API.
Active Ingredient Strength Primary Clinical Function Ledipasvir USP/Ph.Eur. 90 mg Global Hepatology Standard: The definitive daily dose required to maintain constant, paralyzing pressure on the NS5A viral protein across the entire 12-to-24 week curative cycle. Excipients Copovidone / Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Solubility Enhancer / Diluent / Superdisintegrant / Lubricant / Film-Coating (Engineered specifically utilizing Amorphous Solid Dispersion techniques with Copovidone to force the highly insoluble Ledipasvir to dissolve instantly in gastric fluid, guaranteeing maximum systemic bioavailability) *Pack Sizes: Bottles of 28 or 10×10 Blisters (Optimized specifically for strict 4-week dispensing intervals to match custom DAA combination regimens).
Leflunomide Tablets
FreeProduct Composition & Available Portfolio Strengths
We supply Leflunomide across the complete compendial strength matrix, enabling clinicians to manage both rapid initial loading cycles and long-term low-dose maintenance blocks.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Leflunomide USP / BP / IP 10 mg Oral Solid Film-Coated Tablet Low-Dose Maintenance: Calibrated for mild-to-moderate maintenance blocks or patients exhibiting sensitive hepatic profiles. Leflunomide USP / BP / IP 20 mg Oral Solid Film-Coated Tablet The Core Commercial Volume: First-line international standard daily maintenance dose for active Rheumatoid and Psoriatic Arthritis. Leflunomide USP / BP / IP 100 mg Oral High-Mass Solid Tablet Initial Loading Regimen: High-potency format utilized exclusively for the rapid 3-day initial tissue saturation phase. Lenalidomide Capsules
FreeLenalidomide capsules (brand name Revlimid) are a potent immunomodulatory medication used to treat certain types of cancers, such as multiple myeloma and myelodysplastic syndromes.
Letrozole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the micro-dosed endocrine disruptor.
Active Ingredient Strength Primary Clinical Function Letrozole USP/Ph.Eur. 2.5 mg Global Oncology & Fertility Standard: The universal therapeutic unit utilized for 5-to-10 year daily adjuvant breast cancer therapy, or short 5-day cyclic dosing for ovulation induction. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Sodium Starch Glycolate / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Glidant / Slipper-Coating (Engineered specifically using elite geometric dilution to ensure the microscopic 2.5mg active payload is flawlessly distributed throughout the tablet, guaranteeing absolute content uniformity) *Pack Sizes: 10×10 Blisters or Bottles of 30 (Optimized specifically for strict, heavily monitored chronic oncology dispensing or monthly fertility cycles).
Levamisole Hydrochloride veterinary injection
FreeComposition
Levamisole Hydrochloride INJ. 30ML
Usage: – It is typically administered as an injectable solution or added to the animal’s feed.
Category: – parasitic infections veterinary injection
Therapeutic category: –parasitic infections veterinary injection
Levamisole Tablets
FreeProduct Composition & Available Strengths
We supply Levamisole Hydrochloride across the two primary compendial configurations required to execute precise pediatric deworming courses or adult high-mass therapeutic maintenance.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Levamisole Hydrochloride USP / BP / IP 50 mg Oral Solid Uncoated / Chewable Tablet Pediatric Deworming & Titration: Low-dose format calibrated for exact mass titration in pediatric ascariasis or low-dose immunomodulatory courses. Levamisole Hydrochloride USP / BP / IP 150 mg Oral Solid Compressed Tablet The Core Commercial Volume: High-potency, single-dose adult baseline format optimized for rapid mass community deworming campaigns. Levetiracetam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Colorless Solution in glass vials.
Active Ingredient Strength Concentration Levetiracetam USP/BP 500 mg 100 mg/ml (in 5 ml Vial) Excipients Sodium Acetate / Glacial Acetic Acid Buffer / pH Adjuster (5.5) *Pack Sizes: Tray of 5 Vials, 10 Vials, or Single Vial packs.
Levocarnitine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Colorless Solution in glass ampoules or vials.
Active Ingredient Strength Concentration Levocarnitine USP/BP 1 Gram (1000 mg) 200 mg/ml (in 5 ml Ampoule) Excipients Water for Injection pH Adjusted (6.0 – 6.5) *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or Single Use Vials.
Levocetirizine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The small, easy-to-swallow tablets are engineered for rapid disintegration to facilitate quick relief from acute allergic flares.
Active Ingredient Strength (Standard) Therapeutic Role Levocetirizine Dihydrochloride BP/USP 5 mg Potent H1-Receptor Antagonist Excipients Q.S. Microcrystalline Cellulose / Lactose Diluent & Disintegrant Coating Agent Q.S. Opadry® White Protective Film Coating Levofloxacin injection
FreeComposition
Levofloxacin Hemihydrate, 500mg + Sodium Chloride IP
900mg & Water for injection IP q.s
Levofloxacin 500mg & Dextrose Anhydrous 5.0% w/v injection
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
Levofloxacin Tablets
FreeProduct Composition & Available Portfolio
We manufacture Levofloxacin across the complete, internationally standardized therapeutic spectrum to accommodate customized tissue-saturation requirements and specific treatment durations.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Levofloxacin Hemiandrous / Monohydrate USP / BP / IP 250 mg Oral Solid Film-Coated Tablet Uncomplicated Infections: For standard low-dose management of uncomplicated urinary tract infections (UTIs) and acute bacterial sinusitis. Levofloxacin Hemiandrous / Monohydrate USP / BP / IP 500 mg Oral Solid Film-Coated Tablet The Core Commercial Volume: First-line international standard for community-acquired pneumonia (CAP), skin structures, and acute pyelonephritis. Levofloxacin Hemiandrous / Monohydrate USP / BP / IP 750 mg Oral High-Potency Solid Tablet Intensive High-Dose Short-Course: Calibrated for nosocomial pneumonia, complicated skin infections, and advanced multi-drug resistant (MDR) regimens. Levonorgestrel Emergency Contraceptive Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Single-Dose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the potent steroid molecule.
Active Ingredient Strength Primary Clinical Function Levonorgestrel USP/Ph.Eur. 1.5 mg Global Emergency Contraceptive Standard: A massive, single-dose payload designed to instantly halt ovulation within the critical 72-hour post-coital window. Excipients Lactose Monohydrate / Maize Starch / Povidone K30 / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered specifically utilizing advanced micronized API to ensure ultra-rapid gastric dissolution, guaranteeing the hormone hits the bloodstream fast enough to beat the LH surge) *Pack Sizes: 1-Tablet Blister Packs (Optimized specifically for discrete, over-the-counter (OTC) retail and single-dispense NGO crisis kits).
Levosulpiride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the benzamide derivative.
Active Ingredient Strength Primary Clinical Function Levosulpiride USP/Ph.Eur. 25 mg Global Gastroenterology Standard: Base therapeutic unit taken prior to meals for the rapid relief of functional dyspepsia, bloating, and mild gastroparesis. Levosulpiride USP/Ph.Eur. 50 mg / 75 mg Psychiatric & Severe Dysmotility Standard: High-efficacy adult therapy used for severe, treatment-resistant diabetic gastroparesis or utilized by psychiatrists for somatoform disorders and mild depression. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Superdisintegrant / Binder / Glidant (Engineered specifically without heavy polymeric retardants to guarantee immediate, complete gastric dissolution within 10 to 15 minutes of ingestion, preparing the stomach for the incoming meal) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, meal-dependent acute and chronic dispensing regimens).
Levothyroxine Tablet
FreeProduct Composition & Comprehensive Portfolio Range
Because thyroid replacement demands hyper-specific, patient-tailored titrations, we manufacture the entire internationally recognized microgram ($\mu\text{g}$) matrix.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Levothyroxine Sodium USP / BP / IP 25 mcg / 50 mcg Oral Solid Uncoated Micro-Tablet Pediatric & Geriatric Initialization: For delicate low-dose titration in elderly cardiac profiles or initial pediatric replacement. Levothyroxine Sodium USP / BP / IP 75 mcg / 88 mcg / 100 mcg Oral Solid Uncoated Micro-Tablet The Core Commercial Volume: Standard adult maintenance strengths for matching routine daily baseline metabolic deficiencies. Levothyroxine Sodium USP / BP / IP 112 mcg / 125 mcg / 137 mcg Oral Solid Uncoated Micro-Tablet Precision Step-Up Adjustments: Calibrated strengths engineered to adjust plasma levels without requiring multiple or split tablets. Levothyroxine Sodium USP / BP / IP 150 mcg / 175 mcg / 200 mcg Oral High-Potency Micro-Tablet Advanced Suppression Maintenance: For severe profound hypothyroidism, total thyroidectomy recovery, and thyroid cancer suppression therapy. Lidocaine 2% Ampoules
FreeProduct Composition & Strength
We supply this product as a Sterile, Preservative-Free Solution in glass ampoules.
Active Ingredient Strength Total Content (2ml) Lidocaine Hydrochloride USP/BP 2% (20 mg/ml) 40 mg Total Content (5ml) 2% (20 mg/ml) 100 mg Excipients Sodium Chloride / Water for Injection Isotonic Solution *Available in 2ml, 5ml, and 10ml Type I Glass Ampoules.
Lidocaine Cartridges
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Type I Glass Cartridges.
Active Ingredients Strength Cartridge Volume Lidocaine Hydrochloride 2% (20 mg/ml) 1.8 ml / 2.2 ml Adrenaline (Epinephrine) 1:80,000 / 1:100,000 – Stabilizer Sodium Metabisulfite Antioxidant *Pack Sizes: Box of 50 or 100 Cartridges (Blister packed for sterility).
Lidocaine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Multi-dose Vials.
Active Ingredient Strength Common Application Lidocaine Hydrochloride 1% (10 mg/ml) Infiltration / Minor Suturing / Diagnostic Blocks Lidocaine Hydrochloride 2% (20 mg/ml) Major Nerve Blocks / Epidural / Anti-arrhythmic Excipients Sodium Chloride / Methylparaben (in vials) Isotonicity / Preservative *Available in preservative-free (PF) versions for spinal/epidural use.
Lignocain with Adrenaline veterinary injection
FreeComposition
Lignocain with Adrenaline VET 30ML
Usage: –combination medication commonly used in veterinary medicine for various purposes.
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
Lignocaine Adrenaline Dental Cartridges
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Cartridges with siliconized plungers.
Active Ingredients Strength Standard Cartridge Volume Lignocaine Hydrochloride 2% (20 mg/ml) 1.8 ml (Standard) Adrenaline (Epinephrine) 1:80,000 / 1:100,000 2.2 ml (Extended) Excipients Sodium Metabisulfite / NaCl Antioxidant / Isotonicity *Pack Sizes: Box of 50 Cartridges or 100 Cartridges (Blister packed).
Lignocaine Hydrochloride Injection
FreeComposition
Each ml Contains : Lignocaine Hydrochloride I.P. …21.33 mg
Sodium Chloride I.P. ……….. 6 mg
Methyl Paraben I.P ………… 1 mg
Water for Injection I.P. Q.S.Each ml Contains :
Lignocaine Hydrochloride I.P. ..21.33 mg
Adrenaline (As Adrenaline Bitartrate I.P)
……………………………………………0.01mg
Sodium Metabisulphate I.P. …… 1 mg
Methyl Paraben I.P ……… 1 mg
( As Preserva9ve )
Water for Injection I.P. Q.S.Usage: – It is primarily used to induce local anesthesia, meaning it temporarily numbs a specific area of the body
Category: –administered via injection
Therapeutic category: –anesthetic 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
Lignocaine Injection
FreeLignocaine injection (also known as Lidocaine) is a sterile, aqueous solution primarily used as a local anaesthetic and antiarrhythmic agent. Its composition varies depending on whether it is a single-dose or multi-dose formulation and whether it includes a vasoconstrictor.
Linagliptin & Metformin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the highly hygroscopic combination.
Active Ingredient Strength Primary Clinical Function Linagliptin / Metformin HCl (IR) 2.5 mg / 500 mg
2.5 mg / 850 mg
2.5 mg / 1000 mgTwice-Daily Standard: Immediate-release units designed to be taken twice a day with meals to provide rapid, meal-time incretin spikes alongside baseline hepatic suppression. Linagliptin / Metformin HCl (ER) 5 mg / 1000 mg (ER) Once-Daily Premium Standard: High-efficacy Extended-Release therapy designed for ultimate patient compliance, delivering the full daily dose of Linagliptin while slowly trickling Metformin into the gut over 24 hours to prevent severe gastrointestinal side effects. Excipients Hypromellose (HPMC) / Copovidone / Microcrystalline Cellulose / Magnesium Stearate / Premium Moisture-Barrier Film ER Polymer / Binder / Diluent / Lubricant (Engineered utilizing elite Bilayer Rotary Presses to physically separate the delicate 2.5mg/5mg Linagliptin dose from the massive, moisture-drawing Metformin layer, preventing cross-degradation) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 60 (Optimized specifically for strict, massive-volume chronic diabetic dispensing regimens).
Linagliptin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Shielded Film-Coated Tablet, packed exclusively in highly secure Alu-Alu blister strips to ensure the absolute chemical stability of the delicate API.
Active Ingredient Strength Primary Clinical Function Linagliptin USP/Ph.Eur. 5 mg The Universal Standard: A single, high-efficacy maintenance dose that applies to all adult patients, regardless of age, hepatic function, or severe renal impairment. Excipients Mannitol / Pregelatinized Starch / Copovidone / Magnesium Stearate / Premium Opadry Film Diluent / Disintegrant / Binder / Moisture-Barrier Coating (Engineered specifically without highly hygroscopic components to prevent moisture absorption, ensuring rapid disintegration and maximum bioavailability of the 5mg payload) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, massive-volume chronic diabetic dispensing regimens).
Lincomycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Vials.
Active Ingredient Strength Volume Lincomycin Hydrochloride USP/BP 600 mg 2 ml Ampoule (300 mg/ml) – Standard Lincomycin Hydrochloride USP/BP 300 mg 1 ml Ampoule (300 mg/ml) – Pediatric Preservative Benzyl Alcohol 0.945% v/v *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Lincomycin Injection
FreeComposition
Each 2 ml Contains: Lincomycin Hydrochloride I.P. Equi. To
Lincomycin Base 300 mg.
Benzyl Alcohol I.P. 9 mg
Water for Injection I.P. Q.S.Usage: – used for the treatment of various bacterial infections
Category: – anti bacteria injection
Therapeutic category: – susceptible bacteria.
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
Linezolid injection
FreeComposition
Linezolid 600mg &
Dextrose Anhydrous 5% w/v injection
Usage: – Treat different types of bacterial infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Linezolide Tablets
FreeLinezolide Tablets
Each Film Coated Tablet Contains
Linezolide 600 mgUsage: – Treat different types of bacterial infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotics
Lisinopril Tablet
FreeProduct Composition & Available Portfolio Range
We manufacture Lisinopril in exact, compendial strengths calibrated to support initial introductory titration up to high-potency cardioprotective maintenance blocks.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Lisinopril Anhydrous / Dihydrate USP / BP / IP 5 mg Oral Solid Uncoated Tablet Initial Titration: For low-dose introductory management, pediatric hypertension, or initial combination therapy initiation. Lisinopril Anhydrous / Dihydrate USP / BP / IP 10 mg Oral Solid Uncoated Tablet Core Commercial Volume: Standard international baseline daily dose for mild-to-moderate chronic essential hypertension. Lisinopril Anhydrous / Dihydrate USP / BP / IP 20 mg Oral High-Potency Solid Tablet Advanced Cardioprotection: High-strength configuration calibrated for severe heart failure management and post-infarction survival optimization. Lithium Carbonate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the controlled-release polymers.
Active Ingredient Strength Primary Clinical Function Lithium Carbonate USP/Ph.Eur. 300 mg (IR) Acute Mania Standard: Immediate-release base unit used for the rapid, aggressive titration of serum lithium levels during an active, severe manic episode. Lithium Carbonate USP/Ph.Eur. 400 mg / 450 mg (ER/SR) Global Maintenance Standard: Extended-release therapy designed to flatten the pharmacokinetic curve, preventing toxic blood spikes and minimizing severe hand tremors and nausea during lifelong maintenance therapy. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Sodium Starch Glycolate / Magnesium Stearate / Premium Opadry Film Hydrophilic ER Polymer / Diluent / Disintegrant / Lubricant (Engineered specifically using high-shear wet granulation to form a highly reliable, slow-eroding matrix that trickles the elemental lithium into the bloodstream over 12 hours) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict, massive-volume lifelong psychiatric dispensing regimens).
Liv 52 tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Standardized Herbal Matrix Tablet, packed exclusively in highly secure, moisture-resistant PVC/PVDC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly oxidative botanical alkaloids.
Standardized Botanical Extract Target Biomarker Primary Clinical Function Milk Thistle Ext. (Silybum marianum) Standardized to 70% Silymarin (140 mg) The Antioxidant Anchor: Massive glutathione restoration and hepatocyte membrane stabilization. Andrographis paniculata (Kalmegh) Ext. Standardized to 10% Andrographolides The Choleretic Catalyst: Potent antiviral properties (Hepatitis) and violent stimulation of bile flow to flush out hepatic toxins. Phyllanthus niruri (Bhumyamalaki) Ext. Standardized Bitters The Viral Blocker: Clinically documented to suppress the replication of the Hepatitis B virus and protect against drug-induced liver injury (DILI). Boerhavia diffusa (Punarnava) Ext. Standardized Alkaloids The Hepatic Diuretic: Reduces liver enlargement (hepatomegaly) and flushes out excess fluid accumulation (ascites) caused by liver failure. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Film-Coating (Engineered specifically to lock out atmospheric moisture—which destroys botanical extracts—and completely mask the intensely bitter taste of Kalmegh and Silymarin) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict 3-to-6 month chronic hepatology dispensing regimens).
Loperamide Capsules
FreeLoperamide capsules (most commonly known by the brand name Imodium) are an anti-diarrheal medication used to slow down an overactive bowel. They contain a specific active salt and various inactive ingredients that form the capsule and stabilize the medicine
Loperamide Tablet
FreeProduct Composition & Configuration
We supply Loperamide Hydrochloride in the internationally standardized 2 mg therapeutic dosage configuration, engineered for rapid disintegration and fast symptomatic relief.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Application Loperamide Hydrochloride USP / BP / IP 2 mg Oral Solid Immediate-Release Uncoated Tablet Fast-Acting Anti-Diarrheal: Non-specific acute diarrhea management, chronic diarrheal stabilization, and ileostomy output reduction. Excipients Pharma Grade Lactose Monohydrate, Microcrystalline Cellulose, Corn Starch, Magnesium Stearate The Disintegration Scaffold: Optimized matrix for high mechanical stability and rapid water wicking. Lopinavir & Ritonavir Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically Yellow, Oval). The proprietary matrix ensures high bioavailability of poorly soluble Lopinavir.
Active Ingredient Strength (Standard) Therapeutic Role Lopinavir USP/BP 200 mg HIV-1 Protease Inhibitor Ritonavir USP/BP 50 mg Pharmacokinetic Booster (Pediatric Variant) 100 mg Lopinavir + 25 mg Ritonavir Pediatric HIV Management Excipients Q.S. Copovidone / Sorbitan Monolaurate / Silica Solubility Enhancers Loratidine Tablet
FreeProduct Composition & Available Strengths
We supply Loratadine in the internationally recognized 10 mg therapeutic dosage configuration, optimized for maximum daily compliance and clean absorption kinetics.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Application Loratadine USP / BP / IP 10 mg Oral Solid Immediate-Release Uncoated Tablet 24-Hour Allergy Control: Treatment of allergic rhinitis (hay fever), chronic idiopathic urticaria (hives), and ocular allergic reactions. Excipients Pharma Grade Lactose Monohydrate, Corn Starch, Magnesium Stearate The Disintegration Scaffold: Optimized matrix for high mechanical stability during bulk shipping and rapid water-wicking in the gut. Lorazepam Tablet
FreeProduct Composition & Available Strengths
We supply Lorazepam across the complete, internationally standardized therapeutic spectrum to allow for safe dose titration and exact behavioral control.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Target Lorazepam USP / BP / IP 0.5 mg Oral / Sublingual Micro-Tablet Mild Anxiety & Pediatric Titration: For delicate introductory dosing and generalized anxiety management. Lorazepam USP / BP / IP 1.0 mg Oral / Sublingual Micro-Tablet Foundation Anxiolytic / Insomnia: Standard baseline dosage for acute panic control and pre-operative sedation. Lorazepam USP / BP / IP 2.0 mg Oral High-Potency Solid Tablet Critical Care Stabilization: For intensive management of acute manic states, alcohol withdrawal delirium, and status epilepticus. Losartan Potassium Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically Yellow or White, Oval). The coating protects the hygroscopic Losartan from moisture.
Active Ingredient Strength (Standard) Therapeutic Role Losartan Potassium USP/BP 50 mg Vasodilator (ARB) Hydrochlorothiazide USP/BP 12.5 mg Diuretic (Thiazide) (High Strength Variant) 100 mg Losartan + 25 mg HCTZ Severe Hypertension Excipients Q.S. Microcrystalline Cellulose / Lactose / Magnesium Stearate Filler / Lubricant Losartan Potassium, Amlodipine Besylate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Yellow, Oval/Round). The formulation uses the Besylate salt of Amlodipine for maximum stability.
Active Ingredient Strength (Standard) Therapeutic Role Losartan Potassium USP/BP 50 mg Vasodilator (ARB) Amlodipine Besylate USP/BP 5 mg (Eq. to Base) Vasodilator (CCB) (High Strength Variant) 50 mg Losartan + 10 mg Amlodipine
100 mg Losartan + 5 mg AmlodipineResistant Hypertension Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Filler / Super-Disintegrant Losartan Tablet
FreeProduct Composition & Available Strengths
We supply Losartan Potassium across the complete, internationally recognized therapeutic range to facilitate progressive dose titrations and precise maintenance regimens.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Losartan Potassium USP / BP / IP 25 mg Oral Solid Film-Coated Tablet Pediatric & Low-Dose Titration: For introductory pediatric hypertension care or initial combination-therapy building. Losartan Potassium USP / BP / IP 50 mg Oral Solid Film-Coated Tablet Core Commercial Volume: Standard international baseline daily dose for mild-to-moderate chronic essential hypertension. Losartan Potassium USP / BP / IP 100 mg Oral High-Potency Solid Tablet Maximal Saturation Maintenance: For advanced hypertensive management, diabetic nephropathy progression delay, and stroke risk reduction in left ventricular hypertrophy. Magnesium Sulphate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Hypertonic Solution in Glass Ampoules.
Active Ingredient Concentration Strength (per 2ml) Magnesium Sulphate BP/USP 50% w/v (Standard) 1 Gram (in 2 ml) Magnesium Sulphate BP/USP 25% w/v 0.5 Gram (in 2 ml) Magnesium Sulphate BP/USP 10% w/v 2 Grams (in 20 ml) Osmolarity Approx. 4060 mOsmol/L Highly Hypertonic *Pack Sizes: Tray of 10 Ampoules, 25 Ampoules, or 100 Ampoules.
Maxgalin
FreeMaxgalin is a brand of medication manufactured by Sun Pharmaceutical Industries Ltd., primarily used to treat neuropathic (nerve) pain, fibromyalgia, and certain types of seizures.
Mebendazole Tablet
FreeProduct Composition & Available Formats
We supply Mebendazole across the two primary compendial configurations required to execute either targeted individual eradication or high-velocity single-dose mass eradication protocols.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Mebendazole USP / BP / IP 100 mg Oral Solid Chewable / Dispersible Tablet Targeted Multi-Dose Therapy: Standard baseline format for individual 3-day courses targeting specific multi-worm infestations (Pinworms, Roundworms, Hookworms). Mebendazole USP / BP / IP 500 mg High-Mass Oral Solid Single-Dose Tablet Mass Public Health Eradication: High-potency, single-dose format engineered for rapid deployment in mass community deworming campaigns. Mebeverine Tablet
FreeProduct Composition & Available Formats
We supply Mebeverine Hydrochloride in both rapid-acting immediate-release and advanced continuous-release configurations to accommodate customized patient compliance tracking.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Mebeverine Hydrochloride IP / BP / USP 135 mg Oral Solid Immediate-Release Film-Coated Tablet Targeted Acute Dosing: Fast-acting formulation designed for standard three-times-daily administration prior to localized food triggers. Mebeverine Hydrochloride IP / BP / USP 200 mg SR Sustained-Release Hydrophilic Polymer Matrix Tablet / Capsule Continuous 24-Hour Coverage: Premium, once- or twice-daily formulation engineered to release active molecules continuously, eliminating nocturnal spikes and maximizing compliance. Medroxyprogesterone Acetate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Micronized Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the delicate steroid molecule.
Active Ingredient Strength Primary Clinical Function Medroxyprogesterone Acetate USP/Ph.Eur. 2.5 mg / 5 mg HRT Maintenance Standard: Continuous or sequential low-dose therapy for the prevention of endometrial hyperplasia in postmenopausal women receiving estrogen. Medroxyprogesterone Acetate USP/Ph.Eur. 10 mg Acute Gynecology Standard: High-efficacy adult dosing for the rapid arrest of abnormal uterine bleeding and the induction of withdrawal bleeding in secondary amenorrhea. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Lubricant (Engineered specifically utilizing advanced micronized API to overcome the severe hydrophobicity of the steroid, ensuring maximum, predictable gastric absorption) *Pack Sizes: 10×10 Blisters or 14-Day Calendar Packs (Optimized specifically for strict cyclic or continuous gynecological dispensing regimens).
Medroxyprogesterone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Aqueous Suspension in glass vials or prefilled syringes.
Active Ingredient Strength Volume Medroxyprogesterone Acetate USP/BP 150 mg 1 ml Vial (Standard Contraceptive) Medroxyprogesterone Acetate USP/BP 500 mg / 1000 mg High-Dose (Oncology Use) Excipients Polyethylene Glycol / Polysorbate 80 Suspending Agents *Pack Sizes: Single Vial with Syringe, or Tray of 25/50 Vials for Tenders.
Mefanamic Acid & Dicyclomine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant PVC/PVDC or Alu-Alu blister strips to ensure the absolute chemical stability of the combined APIs.
Active Ingredient Strength Primary Clinical Function Mefenamic Acid USP/Ph.Eur. 250 mg The Anti-Inflammatory Anchor: Rapidly reduces prostaglandin-induced pain, uterine inflammation, and heavy menstrual bleeding. Dicyclomine Hydrochloride USP/Ph.Eur. 10 mg The Antispasmodic Catalyst: Instantly relaxes violently contracting smooth muscle in the gastrointestinal and biliary tracts, and the uterus. Excipients Microcrystalline Cellulose / Maize Starch / Sodium Starch Glycolate / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant (Engineered specifically to ensure the bulky Mefenamic Acid powder shatters and dissolves instantly upon reaching the gastric fluid, ensuring the 30-minute rapid onset required for acute pain rescue) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-volume, over-the-counter (OTC) or acute prescription dispensing regimens).
Mefenamic Acid & Paracetamol veterinary injection
FreeComposition
Mefenamic Acid & Paracetamol INJ. 30 ML
Mefenamic Acid & Paracetamol INJ. 100 ML
Usage: – Always consult with a veterinarian before using any medication in animals.
Category: – Anti Analgesic veterinary injection
Therapeutic category: – NSAID, Analgesic, veterinary 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
Mefenamic Tablet
FreeProduct Composition & Available Strengths
We supply Mefenamic Acid in standard, exact compendial strengths designed to support either acute, low-dose short-term relief or high-potency systemic anti-inflammatory regimens.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Mefenamic Acid IP / BP / USP 250 mg Oral Solid Film-Coated Tablet Acute Titration & Dysmenorrhea: Optimized for quick-onset dosing during the initialization of menstrual pain management or mild dental distress. Mefenamic Acid IP / BP / USP 500 mg Oral Solid Film-Coated Tablet High-Potency Stabilization: Standard international baseline strength for functional menorrhagia (heavy bleeding), osteoarthritis flare-ups, and severe acute musculoskeletal pain. Mefloquine Tablet
FreeProduct Composition & Configuration
We supply Mefloquine Hydrochloride in the internationally standardized strength calibrated for both adult therapeutic clearance and weekly travel prophylaxis.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Application Mefloquine Hydrochloride IP / BP / USP 250 mg
(Equivalent to 228 mg Mefloquine Base)
Oral Solid Uncoated Tablet (Cross-scored for exact pediatric dividing) Dual-Mode Antimalarial: High-dose 3-day treatment for active clearance, or low-dose once-weekly regimen for traveler chemoprophylaxis. Excipients Pharma Grade Microcrystalline Cellulose, Lactose, Magnesium Stearate The Disintegration Core: Engineered for uniform mechanical compression and rapid disintegration. Meloxicam veterinary injection
FreeComposition
Meloxicam VET INJ. 30 ML
Meloxicam VET INJ. 100 ML
Usage: –commonly used in veterinary medicine to alleviate pain and reduce inflammation 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
Meloxicam with Paracetamol veterinary injection
FreeComposition
Meloxicam with Paracetamol VET INJ. 100ML
Usage: – used to manage pain and inflammation 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
Melphalan Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, handler-protective Amber Glass Bottles or specialized Alu-Alu cold-chain blisters to ensure the absolute chemical survival of the highly unstable alkylating agent.
Active Ingredient Strength Primary Clinical Function Melphalan USP/Ph.Eur. 2 mg Global Oncology Standard: Base therapeutic unit allowing for highly precise, weight-based or Body Surface Area (BSA) calculated “pulsed” dosing regimens. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Glidant / Slipper-Coating (Engineered specifically with a heavy film-coat to ensure immediate gastric transit and to completely seal the highly toxic, mutagenic core away from nurses and caregivers) *Pack Sizes: Amber Glass Bottles of 25/50 Tablets (Optimized specifically for strict, highly monitored hematology dispensing regimens).
Memantine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips, frequently customized into 4-week Titration Starter Packs.
Active Ingredient Strength Primary Clinical Function Memantine (as Hydrochloride) USP/Ph.Eur. 5 mg Initiation / Titration Standard: Base therapeutic unit utilized exclusively for the mandatory 4-week step-up protocol to build patient tolerance and prevent severe CNS adverse effects. Memantine (as Hydrochloride) USP/Ph.Eur. 10 mg Global Neurology Standard: High-efficacy adult maintenance dose, typically taken twice daily, for the sustained neuroprotection of the degenerating brain. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Slipper-Coating (Engineered specifically with a heavy, smooth film-coat to ensure immediate gastric transit and absolute ease of swallowing for elderly patients suffering from severe dysphagia) *Pack Sizes: 10×10 Blisters, Bottles of 60, or Customized 28-Day Titration Starter Kits (Optimized specifically for strict chronic geriatric dispensing regimens).
Mercaptopurine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, handler-protective Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the antimetabolite and protect healthcare workers from cytotoxic exposure.
Active Ingredient Strength Primary Clinical Function Mercaptopurine (as Monohydrate) USP/Ph.Eur. 50 mg Global Oncology & Autoimmune Standard: Scored tablets allowing for highly precise, weight-based or Body Surface Area (BSA) based dose titrations in pediatric and adult populations. Excipients Lactose Monohydrate / Maize Starch / Pregelatinized Starch / Magnesium Stearate / Stearic Acid Diluent / Binder / Disintegrant / Lubricant (Engineered specifically using high-containment wet granulation to prevent airborne cytotoxic dust generation during manufacturing, ensuring precise, even API distribution) *Pack Sizes: Bottles of 25/50 or 10×10 Blisters (Optimized specifically for strict, heavily monitored chronic oncology dispensing regimens).
Meropenem & Sulbactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder for Injection in glass vials.
Active Ingredient Strength Role Meropenem USP/BP 1000 mg (1 g) Broad-Spectrum Carbapenem Sulbactam Sodium USP/BP Equivalent to 500 mg Beta-Lactamase Inhibitor Total Strength 1.5 g (1500 mg) Per Single Dose Vial *Pack Sizes: Single Vial with or without Sterile Water for Injection.
Meropenem Injection
FreeMeropenem injection (brand name Keppra) is a broad-spectrum carbapenem antibiotic supplied as a sterile white to pale yellow powder for reconstitution. It is used to treat severe bacterial infections
Meropenem injection
FreeComposition
Meropenem 1 g & Sodium 90.2 mg injection
Usage: – used to treat severe intra-abdominal infections caused by susceptible bacteria
Category: – bacterial injection
Therapeutic category: – 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
Mesalazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, pH-Targeted PR Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly oxidative 5-ASA molecule.
Active Ingredient Strength Primary Clinical Function Mesalazine (5-ASA) USP/Ph.Eur. 400 mg (PR) Initiation / Titration Standard: Base therapeutic unit for mild presentations or pediatric titration in pediatric gastroenterology. Mesalazine (5-ASA) USP/Ph.Eur. 800 mg / 1200 mg (PR) Global Gastroenterology Standard: High-efficacy adult maintenance doses designed to improve patient compliance by drastically reducing the daily pill burden. Excipients Methacrylic Acid Copolymer Type B & C (Eudragit L/S) / Hypromellose / Triethyl Citrate / Iron Oxide Colors / Talc Enteric & Prolonged-Release Polymers / Plasticizer / Glidant (Engineered specifically to form an impenetrable, acid-resistant shield that strictly delays drug release until reaching the high-pH environment of the lower gastrointestinal tract) Metformin Hydrochloride & Glimepiride Tablets
FreeProduct Composition & Strength
We supply this product in Bilayer Tablets or Matrix Tablets packed in Alu-Alu or PVC/PVDC Blisters.
Product Strength Metformin HCl (SR) Glimepiride Common Name 500/1 mg 500 mg 1 mg G1 Tablet 500/2 mg 500 mg 2 mg G2 Tablet 1000/2 mg 1000 mg 2 mg Forte / DS Tablet 1000/4 mg 1000 mg 4 mg High Strength Metformin Hydrochloride & Pioglitazone Tablets
FreeProduct Composition & Strength
We supply this product as Sustained Release (SR) Matrix Tablets packed in Alu-Alu Blisters.
Product Strength Metformin HCl (SR) Pioglitazone Common Name 500/15 mg 500 mg 15 mg Pio-M 15 500/30 mg 500 mg 30 mg Pio-M 30 1000/15 mg 1000 mg 15 mg Pio-M Forte 1000/30 mg 1000 mg 30 mg Pio-M DS Metformin Tablet
FreeProduct Composition & Portfolio Range
We manufacture Metformin SR in the full spectrum of internationally recognized therapeutic strengths, utilizing a specialized slow-release scaffold to reduce dosing frequency to once daily.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Metformin Hydrochloride IP / BP / USP 500 mg Hydrophilic Dual-Polymer Sustained-Release Initial Titration: For low-dose introductory management and early-stage Type 2 stabilization. Metformin Hydrochloride IP / BP / USP 750 mg Hydrophilic Dual-Polymer Sustained-Release Intermediate Scaling: Step-up strength to optimize glycemic indices without increasing tablet count. Metformin Hydrochloride IP / BP / USP 1000 mg Hydrophilic Dual-Polymer Sustained-Release High-Potency Maintenance: Maximizes daily therapeutic saturation in an elegant, once-daily single tablet format. Metformin Tablets
FreeProduct Composition & Available Specifications
We supply Metformin Hydrochloride across the full spectrum of compendial strengths and advanced kinetic delivery platforms to optimize patient compliance and reduce gastrointestinal side effects.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Metformin Hydrochloride USP / BP / IP 500 mg Oral Solid Immediate-Release Film-Coated Tablet Introductory Titration: Baseline format designed for low-dose introductory management and gradual step-up scaling. Metformin Hydrochloride USP / BP / IP 850 mg Oral Solid Immediate-Release Film-Coated Tablet High-Density Single Dose: Intermediate strength optimized for achieving target daily therapeutic thresholds with fewer tablets. Metformin Hydrochloride USP / BP / IP 1000 mg Oral High-Mass Immediate-Release Tablet Maximal Saturation Therapy: High-strength configuration calibrated for advanced glycemic control and high-dose combinations. Metformin Hydrochloride USP / BP / IP 500 mg / 1000 mg SR Extended/Sustained-Release Hydrophilic Polymer Matrix Premium GI-Comfort Compliance: Once-daily formulation utilizing a dual-layer hydrogel matrix to release active drug slowly, completely eliminating gastrointestinal distress. Methimazole Tablets
FreeTechnical & Logistics Specifications
HS Code: 3004.90.39 (Medicaments containing hormones or other products – Antithyroid)
CAS Number: 60-56-0 (Methimazole / Thiamazole)
Dosage Form: Uncoated or Film-Coated Tablet
Packaging: Alu-Alu or Alu-PVC Blisters. Protects the sensitive API from environmental humidity; our high-barrier packaging ensures 24-month stability in Zone IVb tropical climates.
Methimazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the thionamide compound.
Active Ingredient Strength Primary Clinical Function Methimazole (Thiamazole) USP/Ph.Eur. 5 mg Maintenance / Titration Standard: Base therapeutic unit for precisely lowering doses as the patient approaches the euthyroid (normal) state, preventing drug-induced hypothyroidism. Methimazole (Thiamazole) USP/Ph.Eur. 10 mg Initial Suppression Standard: High-efficacy adult therapy for rapidly crashing toxic thyroid hormone levels during severe, active hyperthyroidism. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Odor-Masking Coating (Engineered specifically using strict geometric dilution to ensure the microscopic API dose is flawlessly distributed, and fi lm-coated to mask the compound’s inherent sulfurous taste) Methotrexate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Isotonic Solution (Ready-to-Use) or Lyophilized Powder (High Dose).
Active Ingredient Strength Common Application Methotrexate USP/BP 2.5 mg / ml Low Dose (Rheumatology/Dermatology) Methotrexate USP/BP 25 mg / ml Standard Oncology Dose Methotrexate USP/BP 50 mg / 500 mg / 1 g High Dose MTX (Leukemia Protocols) Preservative Benzyl Alcohol Present in Multi-dose Vials (Avoid in IT use) *Pack Sizes: 2 ml Vial, 20 ml Vial, or 50 ml Vial.
Methotrexate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, handler-protective Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the antimetabolite.
Active Ingredient Strength Primary Clinical Function Methotrexate USP/Ph.Eur. 2.5 mg Global Autoimmune Standard: The absolute foundational unit for Rheumatoid Arthritis and Psoriasis, allowing for highly precise, incremental dose titration. Methotrexate USP/Ph.Eur. 5 mg / 7.5 mg / 10 mg Escalated / Oncology Standard: Higher-dose units for severe, refractory autoimmune disease, Choriocarcinoma, and maintenance therapy in Acute Lymphoblastic Leukemia (ALL). Excipients Lactose Monohydrate / Maize Starch / Pregelatinized Starch / Magnesium Stearate Diluent / Binder / Disintegrant / Lubricant (Engineered specifically using high-containment wet granulation to prevent airborne cytotoxic dust generation during manufacturing, ensuring precise, even API distribution) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, heavily monitored chronic dispensing regimens).
Methoxsalen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Dissolution Tablet or Liquid-Filled Softgel, packed exclusively in highly secure, light-blocking Alu-PVC or Amber Blister strips to ensure the absolute chemical stability of the highly photoactive molecule.
Active Ingredient Strength Primary Clinical Function Methoxsalen (8-Methoxypsoralen) USP/Ph.Eur. 10 mg Global Phototherapy Standard: Weight-based dosing unit designed for exact pharmacokinetic synchronization with scheduled clinical UVA light exposure. Excipients Microcrystalline Cellulose / Pregelatinized Starch / Colloidal Silicon Dioxide / Magnesium Stearate (If Tablet) OR Macrogol (PEG 400) / Gelatin (If Softgel) Fast-Dissolving Carrier / Disintegrant / Glidant (Engineered specifically to guarantee complete gastric breakdown and maximum systemic absorption within 60 to 90 minutes, ensuring the patient is perfectly “primed” for the light booth) *Pack Sizes: Bottles of 30 or 10×10 Blisters (Optimized specifically for strict, monitored bi-weekly dermatological dispensing regimens).
Methyl Cobalamin ,Vitamin B6 & Nicotinamide veterinary Injection
FreeCOMPOSITION
Methyl Cobalamin , Vitamin B6 & Nicotinamide INJ. 10 ML
Methyl Cobalamin , Vitamin B6 & Nicotinamide INJ. 30 ML
Methyl Cobalamin , Vitamin B6 & Nicotinamide INJ. 100 ML
Usage: – injections in veterinary medicine may be used to address specific conditions related to B3 deficiencies or skin disorders in animals.
Category: – injections in veterinary medicine
Therapeutic category: –injections in veterinary medicine
Methyl Cobalmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Rapid-Melt Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of both the delicate coenzyme and the hyper-hygroscopic ODT matrix.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Mecobalamin) Ph.Eur./USP 1500 mcg Global Neurology Standard: Mega-dose adult therapy for the aggressive regeneration of peripheral nerves and immediate correction of severe B12 anemia. Excipients Mannitol / Crospovidone / Microcrystalline Cellulose / Sucralose / Premium Cherry or Berry Flavoring / Magnesium Stearate Fast-Dissolving Carrier / Superdisintegrant / Diluent / Sweetener / Masking Agent (Engineered specifically to instantly melt in the saliva within 10 to 30 seconds, creating a highly palatable, sweet liquid that diffuses instantly into the sublingual capillaries) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology and diabetic dispensing regimens).
Methyl Ergometrine Maleate veterinary injection
FreeComposition
Methyl Ergometrine Maleate VET INJ. 5ML
Usage: –Here are some key points about Methyl Ergometrine Maleate for veterinary use
Category: – Veterinary Supervision
Therapeutic category: –Veterinary Supervision
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
Methyl Ergonovine Maleate Tablet
FreeProduct Composition & Calibration Strength
We manufacture this critical emergency therapeutic in the globally accepted standard micro-dose strength optimized for postpartum routine oral management.
Active Ingredient Common Name Compendial Monograph Standard Strength Primary Clinical Target Methyl Ergonovine Maleate (Methylergometrine Maleate) USP / BP / IP 0.2 mg (200 mcg) The Uterotoner Matrix: Administered orally following initial IV/IM stabilization to maintain uterine tone and prevent bleeding recurrence. Excipients Pharma Grade Lactose, Starch, Povidone binders The Delivery Scaffold: Engineered for rapid physical disintegration and quick mucosal absorption. Methylcobalamin + Pyridoxine + Nicotinamide Injection
FreeComposition
PLUS RF (2 ML) Methylcobalamin 1000 mcg
+ Pyridoxine Hydrochloride 100 mg
+ Nicotinamide 100 mg
+ Benzyl Alcohol IP 2% V/V (as preservative)
+ Water for Injection IP q.s.
Usage: –used to treat or prevent vitamin B12 deficiency, which can lead to neurological issues
Category: – Benzyl Alcohol injection
Therapeutic category: – Benzyl Alcohol
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
Methylcobalamin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Red Solution in amber glass ampoules.
Active Ingredient Strength Volume Methylcobalamin JP/USP 500 mcg 1 ml Ampoule Methylcobalamin JP/USP 1500 mcg (1.5 mg) 1 ml / 2 ml Ampoule (Standard Adult Dose) Methylcobalamin JP/USP 2500 mcg (2.5 mg) High-Dose (Intensive Therapy) Excipients Mannitol / Benzyl Alcohol Stabilizer / Preservative *Pack Sizes: Tray of 5 Ampoules, 10 Ampoules, or 100 Ampoules.
Methylcobalamin, Folic Acid & Pyridoxine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the three distinct vitamin coenzymes.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Active B12) Ph.Eur./USP 1500 mcg Myelin Regenerator: Direct peripheral nerve repair and essential co-factor for homocysteine remethylation. Folic Acid (Vitamin B9) Ph.Eur./USP 5 mg Endothelial Shield: Mega-dose methyl-donor driving DNA synthesis, red blood cell formation, and toxic homocysteine clearance. Pyridoxine Hydrochloride (Vitamin B6) Ph.Eur./USP 3 mg Neurotransmitter Catalyst: Vital co-enzyme for the transsulfuration of homocysteine and the synthesis of GABA/Serotonin. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / Heavy UV-Blocking Coating (Engineered specifically to form an impenetrable light barrier, completely preventing the photolabile degradation of the B12 component) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology dispensing regimens).
Methylcobalamine Folic Acid Pyridoxine Hydrochloride & DHA Capsules
FreeThis combination is a specialized nutritional supplement, often prescribed for nerve health (neuropathy), pregnancy, or cardiovascular support. It combines essential B-vitamins with a crucial fatty acid.Methylcobalamine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the delicate coenzyme.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Mecobalamin) Ph.Eur./USP 500 mcg Maintenance / Hematology Standard: Base therapeutic unit for the treatment of Megaloblastic/Pernicious anemia and general nutritional B12 deficiency. Methylcobalamin (Mecobalamin) Ph.Eur./USP 1500 mcg Global Neurology Standard: Mega-dose adult therapy for the aggressive regeneration of peripheral nerves in Diabetic Neuropathy, Sciatica, and Trigeminal Neuralgia. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / UV-Blocking Coating (Engineered specifically to form a heavy, opaque shield that completely locks out ultraviolet light, preventing the photolabile degradation of the active coenzyme) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology dispensing regimens).
Methyldopa Tablet
FreeProduct Composition & Available Strengths
We supply Methyldopa in standard, exact strengths designed to facilitate the careful, progressive dose titration required in gestational healthcare.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Methyldopa Anhydrous IP / BP / USP 250 mg Oral Solid Film-Coated Tablet (Scored for micro-titration) Initial Titration / Baseline Care: For early-stage gestational hypertension and lower-dose fine-tuning. Methyldopa Anhydrous IP / BP / USP 500 mg Oral Solid Film-Coated Tablet (Engineered for uniform mass release) High-Potency Maintenance: For advanced chronic hypertension during pregnancy and severe pre-eclamptic stabilization. METHYLERGOMETRINE INJECTION
FreeCOMPOSITION
Each ml. contains:Methylergometrine Maleate I.P. 0.2 mg.
Water for Injec9on I.P. Q.S 1 mlUsage: – Control bleeding from the uterus
Category: – Generic Drugs and injection
Therapeutic category: – Generic Drugs
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
Methylprednisolone Acetate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Milky White Suspension in glass vials.
Active Ingredient Strength Standard Use Methylprednisolone Acetate 40 mg / ml Standard IM / Small Joints Methylprednisolone Acetate 80 mg / ml High Dose IM / Large Joints (Knee) Excipients Polyethylene Glycol (PEG) / Myristyl-gamma-picolinium chloride Suspending Agent / Preservative *Pack Sizes: 1 ml Vial, 2 ml Vial, or 5 ml Multi-dose Vial.
Methylprednisolone Sodium Succinate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder requiring reconstitution with the provided solvent.
Active Ingredient Strength Standard Use Methylprednisolone Sod. Succ. 40 mg Local Injection / Minor Allergic Reaction Methylprednisolone Sod. Succ. 125 mg Acute Asthma / Status Asthmaticus Methylprednisolone Sod. Succ. 500 mg / 1000 mg (1 gm) Pulse Therapy (Lupus / Transplant Rejection) Diluent Bacteriostatic Water Provided with Act-O-Vial or Separate Ampoule *Pack Sizes: Single Vial with Diluent.
Methylprednisolone Tablet
FreeProduct Composition & Available Strengths
We supply Methylprednisolone in a comprehensive, internationally standardized range of strengths to facilitate both low-dose chronic maintenance and the high-dose taper packs mandatory in clinical steroid therapy.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Target Methylprednisolone USP / BP / IP 4 mg Oral Solid Uncoated Tablet (Cross-scored for micro-titration) Baseline Dose / Tapering: For rheumatoid arthritis maintenance and step-down dose regimens. Methylprednisolone USP / BP / IP 8 mg Oral Solid Uncoated Tablet (Cross-scored for micro-titration) Intermediate Management: For moderate asthma exacerbations and chronic dermatological conditions. Methylprednisolone USP / BP / IP 16 mg Oral Solid Uncoated Tablet (Cross-scored for flexible division) High-Potency Control: For acute autoimmune flares, immunosuppression in organ transplants, and oncology support. Metoclopramide Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Isotonic Solution in glass ampoules.
Active Ingredient Strength Volume Metoclopramide HCl USP/BP 5 mg / ml 2 ml Ampoule (Total 10 mg) Metoclopramide HCl USP/BP 5 mg / ml 10 ml Multi-dose Vial Preservative Sodium Metabisulfite Antioxidant *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Metoclopramide injecton
FreeComposition
Each ml Contains : Metoclopramide Mono Hydrochloride I.P.
Equi. To Anhydrous Metoclopramide
Hcl…………………………………….. 5mg
Methyl Paraben I.P 0.15 % W/V ( As Preserva9ve )
Propyl Paraben I.P 0.02 % W/V ( As Preserva9ve )
Water for Injec9on I.P. Q.S 10 ml , 30 mlUsage: – Anti-sickness medicine
Category: – Antacid & Anti ulcer injection
Therapeutic category: – Antiprotozoal,Anti Vomiting
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Metoclopramide Tablet
FreeProduct Composition & Packaging Specification
We supply Metoclopramide in the globally standardized therapeutic strength optimized for adult baseline three-times-daily dosage regimens.
Active Ingredient Monograph Calibrated Strength Formulation Delivery Matrix Primary Clinical Function Metoclopramide Hydrochloride USP / BP / IP 10 mg Oral Solid Uncoated Tablet (Scored for micro-dosing titration) The Prokinetic Driver: Accelerates upper gastrointestinal transit and blocks central emetic signals. Excipients Pharma Grade Lactose, Starch, Magnesium Stearate The Core Scaffold: High-solubility matrix engineered for rapid physical disintegration. Metoprolol & Amlodipin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the combined molecules.
Active Ingredient Strength Primary Clinical Function Metoprolol (as Tartrate/Succinate ER) Ph.Eur./USP 25 mg / 50 mg Cardioselective Base: Reduces heart rate, cardiac workload, and neutralizes CCB-induced reflex tachycardia. Amlodipine (as Besylate) Ph.Eur./USP 5 mg Calcium Channel Blocker (CCB): Forces profound peripheral arterial vasodilation, dropping severe blood pressure and relieving coronary spasms. Excipients Microcrystalline Cellulose / Dibasic Calcium Phosphate / Crospovidone / Magnesium Stearate / Premium Opadry Film / Iron Oxide Colors Diluent / Stabilizing Buffer / Superdisintegrant / Lubricant (Engineered specifically using bilayer press technology to physically separate the slightly acidic Metoprolol salt from the basic Amlodipine, preventing destructive chemical cross-talk) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Metoprolol & Ramipril Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly degradable Ramipril molecule.
Active Ingredient Strength Primary Clinical Function Metoprolol (as Succinate/Tartrate) Ph.Eur./USP 25 mg / 50 mg Cardioselective Base: Reduces heart rate, cardiac output, and myocardial oxygen demand; protects against sudden cardiac death. Ramipril Ph.Eur./USP 2.5 mg / 5 mg ACE Inhibitor Driver: Forces profound systemic vasodilation, protects the kidneys (renoprotection), and halts pathological cardiac remodeling. Excipients Microcrystalline Cellulose / Sodium Stearyl Fumarate / Hypromellose / Sodium Bicarbonate / Iron Oxide Colors Low-Moisture Diluent / Lubricant / Film-Coating / Polymeric Stabilizer (Engineered specifically to physically isolate the acidic Ramipril from cross-reacting with the Metoprolol salt, preventing the formation of toxic diketopiperazine impurities) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Metoprolol Tablet
FreeCore Product Catalog:
Active Ingredient Monograph Standard Strengths Dosage Format Primary Clinical Target Metoprolol Tartrate IP/BP/USP 25 mg Immediate-Release Solid Tablet Acute Titration: For fine-tuned early adjustment in arrhythmias and mild hypertension. Metoprolol Tartrate IP/BP/USP 50 mg Immediate-Release Solid Tablet Standard Twice-Daily Blockade: Routine maintenance for Angina Pectoris and post-Myocardial Infarction stabilization. Metoprolol Tartrate IP/BP/USP 100 mg Immediate-Release Solid Tablet High-Threshold Control: For refractory tachyarrhythmias and intensive post-MI clinical management. Metronidazole Capsule 500mg
FreeMetronidazole 500 mg capsules are an antibiotic and antiprotozoal medication used to treat a variety of bacterial and parasitic infections. The capsule contains a specific amount of the active drug and various inactive ingredients that help with its delivery and stability.
Metronidazole injection
FreeComposition
Each 100 ml contains
Metronidazole 100 mg +Sodium Chloride 900 mg
Metronidazole injection is 500 mg to 1 gram
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
Metronidazole Tablet
FreeProduct Composition & Available Strengths
We supply Metronidazole in standard, internationally recognized strengths optimized for adult and pediatric treatment regimens.
Active Ingredient Available Strengths Common Dosage Matrix Primary Clinical Target Metronidazole BP / IP / USP 200 mg Film-Coated / Uncoated Oral Tablet Pediatric & Low-Dose Titration: For delicate adjustments in mild amoebic dysentery or combination protocols. Metronidazole BP / IP / USP 400 mg Film-Coated / Uncoated Oral Tablet Standard Generic Backbone: Standard twice or thrice-daily dosing for dental abscesses and Giardiasis. Metronidazole BP / IP / USP 500 mg High-Potency Oral Tablet Institutional Target: High-volume strength preferred for anaerobic surgical prophylaxis and severe trichomoniasis. Metronidazole Vaginal Tablets
FreeProduct Composition & Strength
We supply this product as compressed Vaginal Tablets (Pessaries) in blister packs.
Active Ingredient Strength (Standard) Form Role Metronidazole IP/BP/USP 500 mg Uncoated / Film Coated Tablet Antiprotozoal / Antibacterial Lactic Acid Q.S. (Optional Additive) pH Regulator Excipients Q.S. Disintegrants / Binders Base for Tablet Midazolam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Immediate-Release Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly soluble maleate salt.
Active Ingredient Strength Primary Clinical Function Midazolam (as Maleate) Ph.Eur./USP 7.5 mg Initiation / Geriatric Standard: Base therapeutic unit for pre-surgical anxiety reduction and sleep induction in elderly or debilitated patients. Midazolam (as Maleate) Ph.Eur./USP 15 mg Global Anesthesiology Standard: High-efficacy adult dose for profound pre-procedural conscious sedation and the treatment of severe, treatment-refractory insomnia. Excipients Microcrystalline Cellulose / Lactose Anhydrous / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Fast-Dissolving Carrier / Superdisintegrant / Lubricant (Engineered specifically to shatter upon contact with gastric fluid, ensuring peak plasma concentration is reached within 20 to 30 minutes) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, highly monitored hospital and short-term dispensing regimens).
Midodrine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Immediate-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly soluble hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Midodrine (as Hydrochloride) USP/Ph.Eur. 2.5 mg / 5 mg Initiation / Titration Standard: Base therapeutic units for careful dose-titration to elevate standing blood pressure without triggering dangerous supine hypertension. Midodrine (as Hydrochloride) USP/Ph.Eur. 10 mg Global Dysautonomia Standard: High-efficacy adult maintenance dose for severe neurogenic orthostatic hypotension. Excipients Microcrystalline Cellulose / Pregelatinized Starch / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Disintegrant / Glidant / Lubricant (Engineered specifically without heavy polymeric retardants to guarantee rapid, complete gastric dissolution, ensuring the prodrug reaches the liver instantly for conversion) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, daytime-only chronic dispensing regimens).
Mifepristone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active synthetic steroid.
Active Ingredient Strength Primary Clinical Function Mifepristone (RU-486) Ph.Eur./USP 200 mg Global Reproductive Standard: High-dose adult therapy for the initiation of medical termination of early intrauterine pregnancy (typically up to 70 days gestation). Excipients Microcrystalline Cellulose / Povidone K30 / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant (Engineered specifically to ensure rapid, complete disintegration in the acidic gastric environment, guaranteeing maximum systemic absorption of the critical 200mg payload) *Pack Sizes: 1-Tablet Blister Packs (Optimized specifically for strict, highly regulated single-dose clinical dispensing protocols).
Minocycline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix ER Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or opaque HDPE bottles to ensure the absolute chemical stability of the photosensitive hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Minocycline (as Hydrochloride) USP/Ph.Eur. 50 mg (ER) Dermatology Maintenance Standard: Long-term, low-dose therapy for controlling inflammatory acne and severe Rosacea with minimal side effects. Minocycline (as Hydrochloride) USP/Ph.Eur. 100 mg (ER) Acute Clearance Standard: High-dose therapy for severe cystic acne breakouts, CA-MRSA skin infections, and Rheumatoid Arthritis flares. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Magnesium Stearate / Premium Opaque Opadry Film Hydrophilic ER Polymer / Diluent / Lubricant / UV-Blocking Coating (Engineered specifically to pace the gastric release over several hours, preventing the rapid blood-brain-barrier saturation that triggers vertigo) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 12-to-16 week chronic dermatology dispensing regimens).
Mirabegron Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix ER Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute physical stability of the extended-release polymers.
Active Ingredient Strength Primary Clinical Function Mirabegron Ph.Eur./USP 25 mg (ER) Initiation / Renal Standard: Base therapeutic unit for assessing patient tolerance and for use in patients with severe renal or hepatic impairment. Mirabegron Ph.Eur./USP 50 mg (ER) Global Urology Standard: High-efficacy adult maintenance therapy for maximum suppression of urge urinary incontinence and detrusor overactivity. Excipients Polyethylene Oxide / Hypromellose (HPMC) / Butylated Hydroxytoluene (BHT) / Magnesium Stearate / Premium Opadry Film Swellable ER Polymer / Hydrophilic Matrix Base / Antioxidant / Lubricant (Engineered specifically to form an impenetrable, slow-eroding gel matrix in the GI tract, strictly metering the release of the active ingredient over 24 hours) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 30 (Optimized specifically for strict 30-day chronic urology dispensing regimens).
Mirtazapine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the tetracyclic compound.
Active Ingredient Strength Primary Clinical Function Mirtazapine Ph.Eur./USP 15 mg Initiation / Maximum Sedation Standard: Base unit. (Clinical Quirk: Due to histamine saturation, the 15mg dose is actually MORE sedating than the higher doses, making it the primary choice for severe insomnia.) Mirtazapine Ph.Eur./USP 30 mg / 45 mg Global Psychiatry Standard: High-efficacy adult maintenance therapy for severe Major Depressive Disorder (MDD). At these doses, increased norepinephrine release counteracts some of the histamine-induced sedation. Excipients Microcrystalline Cellulose / Crospovidone / Mannitol / Aspartame / Magnesium Stearate / Premium Flavoring Diluent / Superdisintegrant / Sweetening Agent / Lubricant (Engineered specifically for rapid gastric or sublingual dissolution, heavily utilizing artificial sweeteners and flavors to completely mask the intensely bitter API for geriatric compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic psychiatric dispensing regimens).
Misoprostol Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets, often hexagonal or scored, to allow for precise dosing. Due to the high potency of the API, we ensure rigorous content uniformity.
Active Ingredient Strength (Standard) Therapeutic Role Misoprostol BP/USP 200 mcg (0.2 mg) Prostaglandin E1 Analogue Excipients Q.S. Microcrystalline Cellulose / HPMC Stabilizing Dispersion Matrix Mitomycin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (Purple/Blue Cake) in amber glass vials.
Active Ingredient Strength Primary Use Mitomycin USP/BP 2 mg Ophthalmic Surgery / Pterygium Mitomycin USP/BP 10 mg Systemic Chemotherapy / Bladder Instillation Mitomycin USP/BP 20 mg / 40 mg High-Dose Bladder Protocols Excipients Mannitol Bulking Agent *Pack Sizes: Single Vial. (Must be handled with cytotoxic precautions).
Modafinil Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White/Off-white, Round or Capsule Shaped). The formulation typically utilizes micronized API to ensure rapid onset.
Active Ingredient Strength (Standard) Therapeutic Role Modafinil USP/BP 100 mg Titration / Mild Cases Modafinil USP/BP 200 mg Standard Adult Dose Excipients Q.S. Lactose Monohydrate / Croscarmellose Sodium Filler / Disintegrant Montelukast Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets for adults (10mg) and Chewable Tablets (4mg/5mg) for pediatric use. The film coating ensures stability against atmospheric moisture.
Active Ingredient Strength (Standard) Therapeutic Role Montelukast Sodium BP/USP 10 mg Leukotriene Receptor Antagonist Excipients Q.S. Lactose Monohydrate / Croscarmellose Sodium Disintegrant & Binder Coating Agent Q.S. Opadry® Beige/Pink Moisture Barrier Film Morphine Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extended-Release Matrix Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the controlled-release polymers.
Active Ingredient Strength Primary Clinical Function Morphine Sulphate USP/Ph.Eur. 15 mg (SR) Initiation / Titration Standard: Base therapeutic unit for opioid-naïve patients starting around-the-clock chronic pain management. Morphine Sulphate USP/Ph.Eur. 30 mg / 60 mg (SR) Global Oncology Standard: High-dose adult maintenance therapy for severe, opioid-tolerant terminal cancer and intractable neuropathic pain. Excipients Hypromellose (HPMC) / Cetostearyl Alcohol / Lactose Monohydrate / Magnesium Stearate / Premium Color-Coded Film Hydrophilic Polymer / Lipophilic Retardant / Diluent / Lubricant (Engineered specifically to form an impenetrable, slow-eroding gel matrix in the GI tract, strictly metering the release of the narcotic over 12 hours) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic oncology dispensing regimens; frequently color-coded by strength to prevent fatal dispensing errors).
Moxifloxacin & Cefixime Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive antibiotic compounds.
Active Ingredient Strength Primary Clinical Function Moxifloxacin (as Hydrochloride) Ph.Eur./USP 400 mg 4th-Gen Fluoroquinolone: Deep tissue and lung penetration to eradicate DNA replication in resistant respiratory and intra-abdominal pathogens. Cefixime (as Trihydrate) Ph.Eur./USP 400 mg 3rd-Gen Cephalosporin: Massive Gram-negative cell wall destruction, specifically targeting enteric pathogens like Salmonella typhi. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to protect the hygroscopic Cefixime Trihydrate and mask the intensely bitter taste of Moxifloxacin) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 7-to-14 day acute critical-care anti-infective dispensing regimens).
Moxifloxacin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Moxifloxacin (as Hydrochloride) Ph.Eur./USP 400 mg Global Pulmonology Standard: High-dose adult therapy for the aggressive eradication of resistant respiratory, skin, and intra-abdominal pathogens. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Lactose Monohydrate / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to protect the highly hygroscopic API and completely mask its intensely bitter taste) *Pack Sizes: 1×5 or 10×10 Alu-Alu Blisters (Optimized specifically for strict 5-to-14 day acute critical-care dispensing regimens).
Moxonidine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Micro-Dosed Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient.
Active Ingredient Strength Primary Clinical Function Moxonidine Ph.Eur./BP 0.2 mg Initiation / Mild Standard: Base therapeutic unit for starting therapy, specifically titrated to assess patient tolerance and prevent initial hypotension. Moxonidine Ph.Eur./BP 0.3 mg / 0.4 mg Global Cardiology Standard: High-efficacy adult maintenance dose for the aggressive management of resistant and metabolic hypertension. Excipients Lactose Monohydrate / Povidone K30 / Crospovidone / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Lubricant (Engineered specifically using strict geometric dilution protocols to ensure the microscopic API dose is flawlessly and evenly distributed throughout the entire tablet batch) *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict chronic cardiology dispensing regimens).
Multivitamin & Multimineral Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Sugar Coated Tablets (typically Red, Maroon, or Brown). The coating is an absolute necessity to prevent the oxidative degradation of vitamins by the mineral salts.
Category Ingredient (BP Grade) Strength (Standard) Fat-Soluble Vitamins Vitamin A (Retinol Acetate/Palmitate) BP 2500 IU / 5000 IU Vitamin D3 (Cholecalciferol) BP 200 IU / 400 IU Vitamin E (Tocopheryl Acetate) BP 10 mg / 15 IU Water-Soluble Vitamins Vitamin B1 (Thiamine Mononitrate) BP 2 mg / 10 mg Vitamin B2 (Riboflavin) BP 2 mg / 10 mg Vitamin B3 (Nicotinamide) BP 25 mg / 50 mg Vitamin B6 (Pyridoxine HCl) BP 1 mg / 3 mg Vitamin B12 (Cyanocobalamin) BP 1 mcg / 15 mcg Folic Acid BP 1 mg Vitamin C (Ascorbic Acid) BP 50 mg / 100 mg Minerals & Trace Elements Ferrous Fumarate / Sulphate BP 30 mg / 50 mg (Elemental Iron) Zinc Sulphate BP 15 mg (Elemental Zinc) Copper Sulphate BP 0.5 mg / 2 mg Selenium (as Sodium Selenite) BP 60 mcg / 70 mcg Iodine (as Potassium Iodide) BP 100 mcg / 150 mcg Multivitamin & Multimineral Tablets (Complete A-Z Formula)
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (typically Red, Maroon, or Brown). The coating is an absolute necessity to prevent the oxidative degradation of vitamins by the mineral salts.
Category Ingredient Strength (Standard) Fat-Soluble Vitamins Vitamin A (Acetate/Palmitate) 2500 IU / 5000 IU Vitamin D3 (Cholecalciferol) 200 IU / 400 IU Vitamin E (Acetate) 10 mg / 15 mg Water-Soluble Vitamins Vitamin B1 (Thiamine Mononitrate) 2 mg / 10 mg Vitamin B2 (Riboflavin) 2 mg / 10 mg Vitamin B6 (Pyridoxine HCl) 1 mg / 3 mg Vitamin B12 (Cyanocobalamin) 1 mcg / 15 mcg Vitamin C (Ascorbic Acid) 50 mg / 100 mg Nicotinamide (Vit B3) 25 mg / 50 mg Folic Acid (Vit B9) 1000 mcg (1 mg) Minerals & Trace Elements Ferrous Sulphate (Iron) 30 mg / 50 mg (Elemental) Zinc Sulphate Monohydrate 15 mg / 22.5 mg (Elemental) Copper Sulphate 0.5 mg / 2 mg Selenium Dioxide 60 mcg / 70 mcg Potassium Iodide 100 mcg / 150 mcg Multivitamin 4G Softgels
Free4G multivitamin softgels are specialized health supplements that get their “4G” name from four key herbal extracts—Ginseng, Green Tea, Ginkgo Biloba, and Grape Seed—combined with Omega-3 fatty acids and a comprehensive range of vitamins and minerals. These softgels are designed to support cardiovascular health, cognitive function, and immunity.
Multivitamin Injection
FreeProduct Composition & Strength
We supply this product as a Dual-Ampoule Set or a Single-Vial Emulsion (depending on market regulation).
Vitamin Group Active Ingredients Standard Adult Dose (per 10 ml) Fat-Soluble Retinol (A) / Ergocalciferol (D) / Tocopherol (E) 3300 IU / 200 IU / 10 IU Water-Soluble (C) Ascorbic Acid (C) 100 mg – 200 mg Water-Soluble (B) Thiamine (B1) / Riboflavin (B2) / Pyridoxine (B6) 3 mg / 3.6 mg / 4 mg Others Niacinamide / Pantothenic Acid / Folic Acid / B12 / Biotin 40 mg / 15 mg / 400 mcg / 5 mcg / 60 mcg *Pack Sizes: Tray of 5 Dual-Ampoules or Box of 10 Vials.
Multivitamin Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (typically Red, Yellow, or Brown). The sugar coating is mandatory to mask the strong odor of B-vitamins and protect the labile Vitamin A and C from oxidation.
Active Ingredient Strength (Standard IP/NFI) Therapeutic Role Vitamin A (Acetate) IP 2500 IU Vision / Immunity Vitamin B1 (Thiamine Mononitrate) IP 2 mg Carbohydrate Metabolism Vitamin B2 (Riboflavin) IP 2 mg Mucosal Health Vitamin B6 (Pyridoxine HCl) IP 1 mg Protein Synthesis Niacinamide IP 25 mg Cellular Energy Calcium Pantothenate IP 5 mg Metabolic Support Vitamin C (Ascorbic Acid) IP 50 mg Antioxidant / Collagen Vitamin D3 (Cholecalciferol) IP 200 IU Bone Mineralization Folic Acid IP 1 mg DNA Synthesis / Anemia Excipients Q.S. Gelatin / Sucrose / Talc Binder / Coating Multivitamin Tablets (Vitamin A, D3 & B-Complex)
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (typically Red, Yellow, or Brown). The sugar coating is critical to mask the strong odor of B-vitamins and protect Vitamin A from oxidation.
Active Ingredient Strength (Standard Prophylactic) Therapeutic Role Vitamin A (Acetate/Palmitate) 2500 IU / 5000 IU Vision / Immunity Vitamin D3 (Cholecalciferol) 200 IU / 400 IU Bone Mineralization Thiamine Mononitrate (Vit B1) 2 mg / 10 mg Nerve Function Riboflavin (Vit B2) 2 mg / 10 mg Cellular Energy Pyridoxine HCl (Vit B6) 1 mg / 3 mg Protein Metabolism Niacinamide 20 mg / 50 mg Skin Health / Energy Calcium Pantothenate 5 mg / 50 mg Metabolic Support Folic Acid 1 mg / 1.5 mg DNA Synthesis Excipients Q.S. Gelatin / Sucrose / Talc Binder / Coating Multivitamin Vitamin & B Complex Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often Red, Maroon, or Yellow) to mask the taste and odor of minerals.
Category Key Ingredients (Standard A-Z Profile) Fat Soluble Vitamins Vitamin A (2500 IU), Vitamin D3 (200 IU), Vitamin E (10 mg) Water Soluble Vitamins Vitamin C (50 mg), B1 (2 mg), B2 (2 mg), B6 (1.5 mg), B12 (1 mcg), Niacinamide (25 mg), Folic Acid (300 mcg), Calcium Pantothenate (5 mg) Essential Minerals Zinc Sulfate (Eq. 10 mg Zinc), Ferrous Fumarate (Eq. 30 mg Iron), Magnesium Oxide (10 mg), Calcium Carbonate (75 mg) Trace Elements Copper, Manganese, Iodine, Selenium (Q.S.) Multivitamins & Multiminerals Capsules
FreeMultivitamin and multimineral capsules contain a broad spectrum of active nutrients designed to fill dietary gaps, along with inactive excipients that provide structure and stability to the capsule. While specific formulations vary by brand and target audience (such as men, women, or seniors), most contain a combination of 13 essential vitamins and several key minerals.
Mycophenolate Mofetil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant and handler-protective Alu-Alu blister strips.
Active Ingredient Strength Primary Clinical Function Mycophenolate Mofetil USP/Ph.Eur. 250 mg Dose-Titration / Pediatric Standard: Base therapeutic unit for precise plasma-level titration and pediatric transplant management. Mycophenolate Mofetil USP/Ph.Eur. 500 mg Global Transplant Standard: High-dose adult maintenance therapy for the aggressive prevention of solid organ rejection. Excipients Microcrystalline Cellulose / Povidone K-90 / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Heavy Film-Coating (Engineered specifically to create a dense, impenetrable barrier over the cytotoxic API core, ensuring absolute handling safety for nurses and pharmacists) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic post-transplant dispensing regimens).
N-Acetyl Cysteine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Effervescent Tablet or Odor-Masked Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant heavy-gauge Alu-Alu or Strip packs to ensure the absolute chemical stability of the highly hygroscopic API.
Active Ingredient Strength Primary Clinical Function N-Acetyl Cysteine (NAC) USP/Ph.Eur. 600 mg Global Pulmonology Standard: High-dose adult therapy for the rapid liquefaction of thick respiratory mucus and systemic antioxidant replenishment. Excipients (Effervescent Matrix) Citric Acid Anhydrous / Sodium Bicarbonate / Sucralose / Premium Orange-Lemon Flavoring / Macrogol 6000 Acid-Base Effervescent Couple / Sweetener / Odor-Masking Flavor / Lubricant (Engineered specifically to trigger a violent, complete dissolution in water within 60 seconds, creating a clear, pleasant-tasting respiratory therapeutic drink) *Pack Sizes: 10-Tablet Tubes, 10×10 Strip Packs, or Alu-Alu Blisters (Optimized specifically to absolutely lock out ambient moisture).
N-Acetylcysteine & Taurine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Odor-Masked Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic and sulfurous active ingredients.
Active Ingredient Strength Primary Clinical Function N-Acetylcysteine (NAC) USP/Ph.Eur. 150 mg Glutathione Precursor: Rapid neutralization of reactive oxygen species (ROS) to protect renal tubules and hepatic lobules. Taurine USP/Ph.Eur. 500 mg Intracellular Osmoregulator: Stabilization of glomerular cell membranes to prevent apoptosis and halt proteinuria. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Vanilla-Flavored Opadry Film Diluent / Superdisintegrant / Glidant / Heavy Odor-Masking Coating (Engineered specifically to lock in the noxious sulfur smell of NAC, ensuring absolute patient compliance for long-term chronic use) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic nephrology dispensing regimens).
Nalidixic Tablet
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The formulation is engineered for rapid disintegration to ensure the active ingredient is quickly processed for renal excretion.
Active Ingredient Strength (Standard) Therapeutic Role Nalidixic Acid BP/USP 500 mg Quinolone Antibacterial Excipients Q.S. Maize Starch / Gelatin Binder & Disintegrant Coating (Optional) Q.S. HPMC / Titanium Dioxide Film Coating Naloxone Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Glass Ampoules or Pre-filled Syringes.
Active Ingredient Strength Format Naloxone Hydrochloride USP/BP 400 mcg (0.4 mg) 1 ml Ampoule (Standard Adult) Naloxone Hydrochloride USP/BP 20 mcg (0.02 mg) 1 ml Ampoule (Neonatal/Pediatric) Excipients Methylparaben / Propylparaben Preservative (in Multi-dose Vials) *Pack Sizes: Tray of 10 Ampoules or Box of 10 Vials.
Naltrexone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Taste-Masked Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Naltrexone Hydrochloride USP/Ph.Eur. 50 mg Global Addiction Standard: Single daily maintenance dose to ensure continuous, 24-hour blockade of opioid receptors and suppression of alcohol cravings. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Crospovidone / Magnesium Stearate / Colloidal Silicon Dioxide / Premium Opadry Film Diluent / Superdisintegrant / Glidant / Heavy Film-Coating (Engineered specifically to completely mask the violently bitter taste of the API, preventing the patient from spitting the pill out and ensuring total compliance) *Pack Sizes: 10×10 Blisters or Bottles of 30/100 (Optimized specifically for strictly monitored, 30-day outpatient rehabilitation dispensing regimens).
Naproxen Sodium Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the hygroscopic sodium salt.
Active Ingredient Strength Primary Clinical Function Naproxen Sodium USP/Ph.Eur. 275 mg
(Equivalent to 250 mg Naproxen base)Acute Mild / OTC Standard: Base therapeutic unit for rapid relief of tension headaches, mild trauma, and OTC fever reduction. Naproxen Sodium USP/Ph.Eur. 550 mg
(Equivalent to 500 mg Naproxen base)Acute Severe Rx Standard: High-dose “loading” therapy to instantly abort severe acute migraines, acute gout flares, and post-surgical pain. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Talc / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to protect the hygroscopic salt from humidity in the blister, but trigger a violent, immediate structural collapse the exact second it hits the stomach) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-turnover acute dispensing and retail pharmacy OTC placement).
Naproxen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient and the protective polymer matrix.
Active Ingredient Strength Primary Clinical Function Naproxen USP/Ph.Eur. 250 mg (EC) Initiation / Mild Standard: Base therapeutic unit for mild musculoskeletal trauma, acute gout, and primary dysmenorrhea. Naproxen USP/Ph.Eur. 500 mg (EC) Global Rheumatology Standard: High-dose adult maintenance therapy for severe Rheumatoid Arthritis, Osteoarthritis, and Ankylosing Spondylitis. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Triethyl Citrate / Magnesium Stearate pH-Dependent Enteric Barrier / Diluent / Superdisintegrant / Plasticizer (Engineered specifically to absolutely block dissolution in the highly acidic stomach, preventing mucosal burns, and rapidly dissolving only in the alkaline duodenum) *Pack Sizes: 10×10 Blisters or Bottles of 100/500 (Optimized specifically for strict chronic orthopedic dispensing regimens and massive government health tenders).
Nateglinide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Disintegrating Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly soluble API.
Active Ingredient Strength Primary Clinical Function Nateglinide Ph.Eur./USP 60 mg Initiation / Mild Standard: Base therapeutic unit for patients nearing their HbA1c goal who only require mild postprandial glycemic control. Nateglinide Ph.Eur./USP 120 mg Global Clinical Standard: Primary adult maintenance dose for severe meal-time spikes, taken immediately before the three main meals of the day. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Glidant (Engineered specifically to shatter and dissolve in the stomach in under 15 minutes, guaranteeing the insulin surge perfectly matches the digestion of the meal) *Pack Sizes: 3×10 or 10×10 Blisters (Optimized specifically for high-turnover diabetic dispensing, as patients consume 3 tablets per day).
Nebivolol & Telmisartan Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic and pH-sensitive active ingredients.
Active Ingredient Strength Primary Clinical Function Nebivolol (as HCl) Ph.Eur./USP 2.5 mg / 5 mg Nitric Oxide Donating Beta-Blocker: Reduces cardiac workload while promoting active peripheral vasodilation and preserving sexual function. Telmisartan Ph.Eur./USP 40 mg Metabolic ARB: Provides sustained 24-hour RAAS blockade and improves cellular insulin sensitivity (PPAR-γ modulation). Excipients Meglumine / Sodium Hydroxide / Microcrystalline Cellulose / Povidone K30 / Polysorbate 80 / Magnesium Stearate Alkalizing Agents (Meglumine) / Diluent / Binder / Surfactant (Engineered specifically to create a hyper-alkaline micro-environment for Telmisartan dissolution, physically isolated from the Nebivolol layer to prevent cross-degradation) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Nebivolol Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dual-Active Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the active ingredients.
Active Ingredient Strength Primary Clinical Function Nebivolol (as HCl) Ph.Eur./USP 5 mg Cardioselective & Vasodilatory Base: Reduces cardiac workload and provides active Nitric Oxide-driven peripheral vasodilation. Hydrochlorothiazide (HCTZ) Ph.Eur./USP 12.5 mg / 25 mg Thiazide Diuretic Driver: Forces the excretion of excess sodium and water, massively amplifying the blood-pressure-lowering effect of the beta-blocker. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Polysorbate 80 / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Wetting Surfactant / Moisture-Barrier Coating (Engineered specifically to protect the highly delicate racemic Nebivolol balance while ensuring rapid, synchronized gastric dissolution of the diuretic) *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Nebivolol Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Low-Dose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Nebivolol (as HCl) Ph.Eur./USP 2.5 mg / 5 mg Global Hypertension Standard: Base therapeutic unit for the continuous, highly tolerated management of essential hypertension. Nebivolol (as HCl) Ph.Eur./USP 10 mg / 20 mg Advanced Cardiac Standard: High-dose maintenance therapy for refractory hypertension and specialized heart failure protocols. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Hypromellose / Polysorbate 80 / Magnesium Stearate Diluent / Superdisintegrant / Wetting Agent / Lubricant (Engineered specifically to ensure rapid, predictable gastric dissolution while protecting the delicate racemic balance of the API) *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict, high-compliance chronic cardiology dispensing regimens).
Nelfinavir Tablet
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. Due to the high dose required for therapeutic efficacy, we ensure the tablet is engineered for ease of swallowing without compromising the structural integrity of the high-API load.
Active Ingredient Strength (Standard) Therapeutic Role Nelfinavir Mesylate USP/BP 250 mg Standard Adult / Pediatric Dose Nelfinavir Mesylate USP/BP 625 mg High-Strength Adult Maintenance Excipients Q.S. Calcium Silicate / Crospovidone Disintegrant & Stabilizer Neomercazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly reactive thionamide molecule.
Active Ingredient Strength Primary Clinical Function Carbimazole Ph.Eur./BP 5 mg Maintenance / Titration Standard: Base therapeutic unit for the gradual tapering of therapy and long-term maintenance of euthyroidism. Carbimazole Ph.Eur./BP 10 mg / 20 mg Acute Initiation Standard: High-dose induction therapy to aggressively shut down severe, life-threatening thyrotoxicosis. Excipients Lactose Monohydrate / Maize Starch / Magnesium Stearate / Povidone K30 / Iron Oxide Yellow (for distinct clinical identification) Diluent / Binder / Lubricant (Engineered specifically for rapid, complete gastric dissolution to achieve peak methimazole blood levels within 1 to 2 hours) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict chronic endocrinology dispensing, as patients initiate on high doses and taper down over many months).
Neomycin Sulphate veterinary injection
FreeComposition
Neomycin Sulphate INJ. 30 Ml
Usage: – use of neomycin in veterinary medicine is similar to its use in humans
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
Neostigmine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Isotonic Solution in glass ampoules or vials.
Active Ingredient Strength Format Neostigmine Methylsulfate USP/BP 0.5 mg / ml 1 ml / 10 ml Vial (Standard) Neostigmine Methylsulfate USP/BP 2.5 mg / ml Concentrate (Rarely used) Excipients Phenol / Methylparaben Preservative (in Multi-dose Vials) *Pack Sizes: Tray of 10 Ampoules or Box of 1/10 Vials.
Neostigmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly hygroscopic bromide salt.
Active Ingredient Strength Primary Clinical Function Neostigmine Bromide Ph.Eur./USP 15 mg Global Clinical Standard: Base therapeutic oral unit for the continuous, meticulously spaced symptomatic management of Myasthenia Gravis. Excipients Lactose Monohydrate / Maize Starch / Povidone K30 / Talc / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered specifically for rapid, predictable gastric dissolution to ensure precise symptom control within 30 to 45 minutes of ingestion) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, high-volume chronic neurology dispensing, as patients may require up to 10-15 tablets per day in divided doses).
Nevirapine Tablet
FreeProduct Composition & Strengths
We supply this antiretroviral therapeutic in the globally accepted standard therapeutic strength optimized for adult combination maintenance therapy.
Active Ingredient Standard Strength Formulation Delivery Matrix Primary Clinical Function Nevirapine Anhydrous IP / BP / USP 200 mg Oral Solid Uncoated Tablet (Scored for flexible pediatric/titration dividing) The NNRTI Anchor: Suppresses viral replication loads when used in combination ARV regimens. Excipients Pharma Grade Lactose, Microcrystalline Cellulose, Sodium Starch Glycolate The Delivery Core: Ensures immediate physical disintegration and release kinetics. Niacinamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Purity Tablet, packed exclusively in highly secure, premium Alu-PVC blister strips or high-density HDPE aesthetic bottles to ensure the absolute chemical stability of the vitamin matrix.
Active Ingredient Strength Primary Clinical Function Niacinamide (Vitamin B3) USP/Ph.Eur. 500 mg Global Premium Dermatology Standard: High-dose adult therapy for systemic acne control, anti-aging ceramide synthesis, and hyperpigmentation reduction. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Stearic Acid / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Lubricant (Engineered specifically for rapid gastric dissolution to ensure peak systemic saturation and rapid delivery to the dermal layers) *Pack Sizes: 10×10 Blisters or Bottles of 60/100 (Optimized specifically for premium OTC retail and daily dermatological regimens).
Nicorandil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Moisture-Shielded Tablet, packed exclusively in highly secure, heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the highly volatile active ingredient.
Active Ingredient Strength Primary Clinical Function Nicorandil Ph.Eur./BP 5 mg Initiation / Titration Standard: Base therapeutic unit for the mandatory slow-titration protocol required to build patient tolerance and prevent severe “nitrate headaches.” Nicorandil Ph.Eur./BP 10 mg / 20 mg Global Cardiology Standard: High-dose adult maintenance therapy for severe, refractory stable angina pectoris. Excipients Maize Starch / Croscarmellose Sodium / Stearic Acid / Mannitol Low-Moisture Diluent / Superdisintegrant / Lubricant (Engineered specifically without hygroscopic binders to guarantee the tablet remains perfectly dry and structurally intact throughout its shelf life) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic cardiology dispensing regimens).
Nicotinamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or high-density HDPE bottles to ensure the absolute chemical stability of the highly soluble vitamin amide.
Active Ingredient Strength Primary Clinical Function Nicotinamide (Niacinamide) USP/Ph.Eur. 250 mg Dermatology / Acne Standard: Base therapeutic unit for the systemic reduction of inflammatory skin lesions and mild nutritional supplementation. Nicotinamide (Niacinamide) USP/Ph.Eur. 500 mg Oncology Prophylaxis / Pellagra Standard: High-dose adult therapy for non-melanoma skin cancer prevention and acute pellagra eradication. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Stearic Acid / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Lubricant (Engineered specifically for rapid, complete gastric dissolution to ensure peak systemic NAD+ saturation within 1 to 2 hours) *Pack Sizes: 10×10 Blisters or Bottles of 60/100 (Optimized specifically for chronic, twice-daily dermatological dispensing regimens).
Nicotinic Acid Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Hydrophilic Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the extended-release polymer.
Active Ingredient Strength Primary Clinical Function Nicotinic Acid (Niacin) USP/Ph.Eur. 500 mg (ER) Initiation / Titration Standard: Base therapeutic unit for the mandatory, slow 4-week dose titration protocol required to build patient tolerance. Nicotinic Acid (Niacin) USP/Ph.Eur. 1000 mg (ER) Global Cardiology Standard: High-dose adult maintenance therapy for severe mixed dyslipidemia and extreme hypertriglyceridemia. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Stearic Acid / Colloidal Silicon Dioxide / Premium Opadry Film Hydrophilic Polymer Matrix / Diluent / Lubricant / Glidant (Engineered specifically to form a viscous, highly controlled gel barrier upon swallowing, metering the API release precisely into the gastrointestinal tract over 8-12 hours) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict chronic cardiology dispensing regimens).
Nicoumalone Tablet
FreeProduct Composition & Calibration Spectrum
We manufacture Nicoumalone in a complete, highly precise range of strengths to allow for the exact dosage adjustments required to maintain narrow therapeutic targets.
Active Ingredient Common Name Compendial Monograph Available Strengths Primary Clinical Application Nicoumalone (Acenocoumarol) BP / IP / USP 1 mg Micro-Titration Phase: For delicate, low-dose fine-tuning in geriatric or sensitive patient profiles. Nicoumalone (Acenocoumarol) BP / IP / USP 2 mg Foundational Maintenance: The standard baseline dose for routine daily thromboembolic prophylaxis. Nicoumalone (Acenocoumarol) BP / IP / USP 3 mg Intermediate Control: For patients requiring step-up adjustment to hit targeted coagulation thresholds. Nicoumalone (Acenocoumarol) BP / IP / USP 4 mg High-Threshold Suppression: For rapid oral loading or patients presenting high chemical resistance to standard doses. Nifedipine Tablet
FreeProduct Composition & Structural Formats
We manufacture Nifedipine across the complete clinical dosage spectrum, utilizing distinct release matrices calibrated for immediate stabilization or sustained, once-daily therapeutic coverage.
Active Ingredient Available Strengths Formulation Matrix Delivery System Primary Clinical Focus Nifedipine IP/BP/USP 10 mg Immediate-Release / Rapid-Onset Film Tablet Acute Titration / Tocolysis: For severe acute hypertension or suppression of premature labor contractions. Nifedipine IP/BP/USP 20 mg Sustained-Release (SR) Retard Matrix Twice-Daily Maintenance: Intermediate control for stable chronic hypertension. Nifedipine IP/BP/USP 30 mg Once-Daily Extended-Release (XR / XL) Matrix First-Line Chronic Care: Continuous 24-hour plasma stabilization for mild-to-moderate hypertension. Nifedipine IP/BP/USP 60 mg Once-Daily Extended-Release (XR / XL) Matrix High-Potency Control: For refractory essential hypertension and severe chronic stable angina pectoris. Nifedipine Tablet
FreeProduct Composition & Structural Formats
We supply Nifedipine in exact, internationally standardized strengths, optimized for immediate-release emergency titration or controlled-release daily maintenance.
Active Ingredient Available Strengths Formulation Mechanism Primary Clinical Target Nifedipine IP / BP / USP 10 mg Immediate or Modified Release Acute Titration / Tocolysis: For rapid blood pressure adjustment or suppression of premature labor. Nifedipine IP / BP / USP 20 mg Sustained / Retard Matrix Daily Maintenance: Continuous 12-to-24-hour plasma concentration for chronic hypertension and angina. Nimesulide ,Paracetamol & Chlorzoxazone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of all three active ingredients.
Active Ingredient Strength Primary Clinical Function Nimesulide BP/Ph.Eur. 100 mg Preferential COX-2 NSAID: Rapid abortion of localized musculoskeletal inflammation and tissue swelling. Paracetamol (Acetaminophen) BP/Ph.Eur. 325 mg Central Analgesic: Synergistic pain threshold elevation and antipyretic control. Chlorzoxazone USP/Ph.Eur. 250 mg Central Muscle Relaxant: Direct inhibition of spinal reflex arcs to break severe, locked muscle spasms. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Premium Opadry Film Diluent / Superdisintegrant / Binder / Moisture-Barrier Coating (Engineered specifically to trigger a violent, immediate structural collapse in the stomach, ensuring all three APIs are absorbed simultaneously for synchronized relief) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute dispensing to ensure patients do not exceed the mandated 15-day Nimesulide therapy limit).
Nimesulide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Rapid-Burst Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient.
Active Ingredient Strength Primary Clinical Function Nimesulide BP/Ph.Eur. 100 mg Global Acute Standard: High-efficacy adult therapeutic unit for the rapid, short-term abortion of acute inflammatory pain. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Docusate Sodium / Povidone K30 / Magnesium Stearate Diluent / Superdisintegrant / Wetting Surfactant / Binder (Engineered specifically to trigger a violent, immediate structural collapse in the stomach, maximizing the drug’s surface area for ultra-fast gastrointestinal absorption) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute dispensing to ensure patients do not exceed the mandated 15-day therapy limit).
Nimesulide, Paracetamol & Serratiopeptidase Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Multi-Particulate Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly delicate enzyme component.
Active Ingredient Strength Primary Clinical Function Nimesulide BP/Ph.Eur. 100 mg Preferential COX-2 NSAID: Rapid abortion of localized musculoskeletal inflammation and tissue pain. Paracetamol (Acetaminophen) BP/Ph.Eur. 325 mg Central Analgesic: Synergistic pain threshold elevation and antipyretic control. Serratiopeptidase (as Enteric-Coated Granules) 15 mg
(Equivalent to 30,000 Serratiopeptidase Units)Proteolytic Enzyme: Direct breakdown of fibrin and inflammatory exudate to physically drain severe localized edema. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate Enteric Polymer Shield / Diluent / Superdisintegrant / Binder (Engineered specifically to protect the enzyme from gastric acid while allowing the analgesics to dissolve instantly in the stomach) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, short-term acute dispensing to ensure patients do not exceed the mandated 15-day Nimesulide therapy limit).
Nitrazepam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active ingredient and prevent unauthorized access.
Active Ingredient Strength Primary Clinical Function Nitrazepam BP/Ph.Eur. 5 mg Initiation / Elderly Standard: Base therapeutic unit for the short-term management of severe insomnia, specifically titrated for elderly patients to prevent next-day falls. Nitrazepam BP/Ph.Eur. 10 mg Severe Psychiatric Standard: Maximum adult dose to force sleep in highly agitated, refractory, or acutely manic patients. Excipients Lactose Monohydrate / Maize Starch / Microcrystalline Cellulose / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Binder / Disintegrant / Lubricant (Engineered specifically for rapid gastric dissolution, inducing sleep within 30 to 60 minutes of ingestion) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 2-to-4 week acute psychiatric dispensing regimens to prevent dependency).
Nitrofurantoin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Dual-Release Capsule or Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the nitrofuran compounds.
Active Ingredient Strength Primary Clinical Function Nitrofurantoin (Macrocrystals) USP/Ph.Eur. 50 mg Prophylactic / Pediatric Standard: Base therapeutic unit for long-term prevention of recurrent UTIs and pediatric dosing. Nitrofurantoin (Macrocrystals 25mg + Monohydrate 75mg) USP 100 mg Global Acute UTI Standard: Premium dual-release adult maintenance dose for the rapid eradication of acute uncomplicated cystitis. Excipients Carbomer 934P / Povidone K30 / Sugar Spheres / Talc / Magnesium Stearate / Titanium Dioxide Hydrophilic Polymer Matrix / Binder / Core Substrate / Glidant (Engineered specifically to form a viscous gel upon swallowing, pacing the gastric release perfectly to prevent nausea while ensuring maximum urinary concentration) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict 5-to-7 day acute urology dispensing regimens).
Nitrofurantoin Tablets
FreeA Nitrofurantoin tablet is an antibiotic specifically used to treat and prevent urinary tract infections (UTIs), such as cystitis. It works by damaging the DNA of bacteria in the urinary tract.
Nitroglycerin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Concentrate for Infusion in glass ampoules or vials. (Must be diluted).
Active Ingredient Strength Total Content Nitroglycerin USP/BP 5 mg/ml 25 mg (in 5 ml Ampoule) Nitroglycerin USP/BP 5 mg/ml 50 mg (in 10 ml Vial) Excipients Propylene Glycol / Ethanol Solubilizers (Volatile) *Pack Sizes: Tray of 5 Ampoules or 10 Vials.
Nitroglycerin Tablet
FreeProduct Composition & Available Strengths
We supply Nitroglycerin Sublingual Tablets in exact, internationally calibrated low-dose strengths to allow for immediate rescue titration during acute ischemic episodes.
Active Ingredient Common Name Compendial Title Available Strengths Primary Clinical Target Nitroglycerin (GTN) Glyceryl Trinitrate IP / BP / USP 0.4 mg Standard Rescue Dose: Preferred international standard for immediate acute angina abortion. Nitroglycerin (GTN) Glyceryl Trinitrate IP / BP / USP 0.5 mg High-Threshold Prophylaxis: Calibrated for heavy coronary spasm management or pre-exertion protection. Norethisterone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly potent steroid hormone.
Active Ingredient Strength Primary Clinical Function Norethisterone Ph.Eur./USP 5 mg Global Gynecology Standard: High-dose therapeutic unit for acute hemorrhage cessation, endometriosis suppression, and menstrual cycle manipulation. Excipients Lactose Monohydrate / Maize Starch / Magnesium Stearate / Povidone K30 Diluent / Binder / Lubricant (Engineered specifically for rapid gastric dissolution to halt acute uterine bleeding within 24-48 hours of the first dose) Pack Sizes: 10×10 Blisters or 3×10 Calendar Packs (Optimized specifically for strict cyclical gynecology dispensing regimens).
Norfloxacin & Tinidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips to ensure the absolute chemical stability of the highly photolabile active ingredients.
Active Ingredient Strength Primary Clinical Function Norfloxacin USP/Ph.Eur. 400 mg Aerobic Gut/UTI Standard: Broad-spectrum eradication of Gram-negative/positive bacteria driving acute gastroenteritis and genitourinary infections. Tinidazole USP/Ph.Eur. 600 mg Anaerobic/Protozoal Standard: Highly tolerable eradication of tissue-invasive amoebas, giardia, and pelvic anaerobes. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Hypromellose / Titanium Dioxide Diluent / Superdisintegrant / Binder / Premium Opaque Film-Coating (Engineered specifically to form an impenetrable barrier that completely masks the notoriously bitter, metallic taste of both APIs, guaranteeing patient compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 5-to-10 day acute anti-infective dispensing regimens).
Norfloxacin Tablet
FreeProduct Composition & Strength
We supply Norfloxacin in the globally standardized therapeutic strength optimized for adult twice-daily dosage regimens.
Active Ingredient Strength (per Tablet) Primary Microbiological Function Norfloxacin USP / BP / IP 400 mg The DNA Gyrase Blocker: Eradicates susceptible urinary and gastrointestinal pathogens. Excipients Pharma Grade The Core Matrix: High-performance binders optimized for rapid tablet dissolution. Nystatin Tablet
FreeProduct Composition & Configuration
We supply this product in the internationally recognized standard therapeutic strength optimized for uniform, localized mucosal distribution.
Active Ingredient Strength (per Tablet) Formulation Delivery System Primary Clinical Function Nystatin IP / BP / USP 100,000 IU Non-Effervescent Local Insert: Designed for slow physical disintegration within vaginal mucosal fluids. The Polyene Fungicide: Eradicates superficial Candida strains locally. Excipients Pharma Grade Modified lactose, starch, and lubricating binding agents. The Comfort Base: Ensures non-irritating, smooth insertion profiles. Ofloxacin & Ornidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips to ensure the absolute chemical stability of the highly photolabile active ingredients.
Active Ingredient Strength Primary Clinical Function Ofloxacin USP/Ph.Eur. 200 mg Aerobic Standard: Broad-spectrum eradication of Gram-negative/positive bacteria driving acute gastroenteritis and genitourinary infections. Ornidazole INN/Ph.Eur. 500 mg Anaerobic/Protozoal Standard: Highly tolerable eradication of tissue-invasive amoebas, giardia, and surgical-site anaerobes. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K30 / Magnesium Stearate / Hypromellose / Titanium Dioxide Diluent / Superdisintegrant / Binder / Premium Opaque Film-Coating (Engineered specifically to form an impenetrable barrier that completely masks the notoriously bitter, metallic taste of both APIs, guaranteeing patient compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-5 day acute anti-infective dispensing regimens).
Ofloxacin & Satranidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the fluoroquinolone and nitroimidazole APIs.
Active Ingredient Strength Primary Clinical Function Ofloxacin USP/Ph.Eur. 200 mg Broad-spectrum fluoroquinolone for the eradication of aerobic bacterial pathogens. Satranidazole INN/Ph.Eur. 300 mg Premium nitroimidazole for the eradication of anaerobic bacteria and protozoa. Excipients Microcrystalline Cellulose / Crospovidone / Magnesium Stearate / Hypromellose Diluent / Superdisintegrant / Lubricant / Premium Film-Coating (Engineered to mask bitterness and ensure immediate gastric dissolution) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for standard 3-to-5 day acute gastrointestinal and pelvic infection regimens).
Ofloxacin injection
FreeComposition
Ofloxacin 200 mg / 100 ml
Usage: – Treat bacterial infections
Category: – Antibiotic injection
Therapeutic category: – Antibiotic
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Ofloxacin Tablets
FreeOfloxacin Tablets 200 mg
Each Filmcoated tablet contains :
Ofloxacin IP 200 mg
Excipients q.sYALLEY FLOX
Ofloxacin Tablets 200mg Each Film coated tablet contains :
Ofloxacin BP 200 mg
Excipients q.sOfnis -200
Ofloxacin Tablets
Each Filmcoated tablet contains :
Ofloxacin BP 200 mgUsage: – Treat bacterial infections
Category: – Antibiotic drugs
Therapeutic category: – Antibiotic
Olanzapine & Fluoxetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Capsule or Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly oxidative Olanzapine molecule.
Active Ingredient Strength Primary Clinical Function Olanzapine Ph.Eur./USP 3 mg / 6 mg / 12 mg Atypical Base: Modulates 5-HT2A/D2 receptors to stabilize severe mood swings and trigger prefrontal synergy. Fluoxetine (as HCl) Ph.Eur./USP 25 mg / 50 mg SSRI Driver: Forces a massive serotonin pool in the synaptic cleft to elevate refractory depressive lows. Excipients Pregelatinized Starch / Croscarmellose Sodium / Microcrystalline Cellulose / Magnesium Stearate / Opadry Film Moisture-Scavenging Diluent / Superdisintegrant / Binder / Premium Oxygen-Barrier Film-Coating (Engineered specifically to physically isolate the highly sensitive Olanzapine from cross-reacting with Fluoxetine) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic psychiatric dispensing regimens).
Olanzapine Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (Yellow Cake) in glass vials.
Active Ingredient Strength Reconstitution Requirement Olanzapine BP/USP 10 mg Requires 2.1 ml of Sterile Water for Injection Excipients Lactose Monohydrate / Tartaric Acid Bulking Agent / Solubilizer *Pack Sizes: Single Vial. (Produces a clear, yellow solution upon reconstitution).
Olanzepine Tablet
FreeProduct Composition & Available Strengths
We supply Olanzapine in standard, exact strengths to facilitate initial titration phases and safe daily maintenance therapy.
Active Ingredient Available Strengths Primary Clinical Target Olanzapine IP / BP / USP 2.5 mg Introductory Titration: For low-dose introductory cycles, elderly adjustment, or sensitive patient profiles. Olanzapine IP / BP / USP 5 mg Standard Maintenance: The baseline daily dosage for long-term schizophrenic and bipolar maintenance. Olanzapine IP / BP / USP 10 mg Acute Crisis Control: High-potency therapeutic dosing to stabilize acute manic or severe psychotic episodes. Olmesartan Medoxomil Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly volatile ester prodrug.
Active Ingredient Strength Primary Clinical Function Olmesartan Medoxomil Ph.Eur./USP 20 mg Initiation / Global Standard: Standard adult starting and maintenance dose for the continuous control of essential hypertension. Olmesartan Medoxomil Ph.Eur./USP 40 mg Severe Refractory Standard: Maximum adult maintenance dose for patients requiring further reduction in blood pressure. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Hydroxypropyl Cellulose / Magnesium Stearate / Titanium Dioxide Low-Moisture Diluent / Binder / Lubricant / Premium Moisture-Barrier Film-Coating (Engineered specifically to lock out ambient humidity and prevent the premature hydrolysis of the medoxomil group prior to ingestion) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Olmesartan, Amlodipine & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, API-Segregated Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of all three active ingredients across their entire shelf life.
Active Ingredient Strength Primary Clinical Function Olmesartan Medoxomil Ph.Eur./USP 20 mg / 40 mg ARB Base: Blocks the renin-angiotensin-aldosterone system (RAAS) and provides critical diabetic renoprotection. Amlodipine (as Besylate) Ph.Eur./USP 5 mg / 10 mg CCB Vasodilator: Forces profound, sustained peripheral arterial relaxation. Hydrochlorothiazide (HCTZ) Ph.Eur./USP 12.5 mg / 25 mg Diuretic Volume Controller: Flushes excess sodium/water and massively amplifies the efficacy of the ARB component. Excipients Silicified Microcrystalline Cellulose / Pregelatinized Starch / Croscarmellose Sodium / Magnesium Stearate / Opadry Protective Film Moisture-Scavenging Diluent / Binder / Superdisintegrant / Premium Film-Coating (Engineered specifically to physically isolate the highly sensitive Olmesartan ester from the alkaline Amlodipine salt to prevent cross-degradation) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Omeprazole & Domperidone Capsules
FreeOmeprazole and Domperidone capsules are a combination medication primarily containing two active salts to treat acid reflux and indigestion.
Omeprazole Capsules
FreeOmeprazole capsules typically contain enteric-coated pellets to prevent the stomach’s acid from breaking down the medication before it can be absorbed in the small intestine.
Omeprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Off-White Cake) in clear glass vials, typically accompanied by a specialized sterile solvent.
Active Ingredient Strength Reconstitution Requirement Omeprazole Sodium USP/BP 40 mg Requires provided 10 ml solvent or specific diluent Excipients Sodium Hydroxide / Disodium Edetate Alkalizing Agent / Stabilizer *Pack Sizes: Single Vial + 10 ml Solvent Ampoule, or Tray of 10 Vials.
Omeprazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Capsule or Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly acid-labile benzimidazole derivative.
Active Ingredient Strength Primary Clinical Function Omeprazole BP/USP/Ph.Eur. 10 mg OTC / Maintenance Standard: Approved unit for over-the-counter frequent heartburn relief and long-term remission maintenance of healed esophagitis. Omeprazole BP/USP/Ph.Eur. 20 mg Global Clinical Standard: Primary adult daily dose for active GERD, gastric ulcers, and standard H. pylori eradication protocols. Omeprazole BP/USP/Ph.Eur. 40 mg Severe Refractory Standard: High-dose therapy for severe erosive esophagitis, NSAID-induced bleeding ulcers, and Zollinger-Ellison Syndrome. Excipients Methacrylic Acid Copolymer / Hypromellose (HPMC) / Sugar Spheres / Macrogol / Titanium Dioxide pH-Dependent Enteric Coating / Sub-coating Barrier / Core Substrate / Plasticizer (Engineered specifically to resist gastric fluid at pH 1.2 but dissolve instantly at duodenal pH 6.8) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 100 (Optimized specifically for strict 14-to-28 day acute GI healing regimens).
Ondansetron injection
FreeComposition
Each ml contains: Ondansetron Hcl
(as dihydrate) Eq. to Ondansetron 2mg ; Water for injection q.s.
Each ml Contains: Ondansetron Hydrochloride
Eq to Ondansetron 2 mg.
Water for Injection Q.S. 2 ml, 4 mlUsage: – Trigger nausea and vomiting
Category: – Antacid & Anti ulcer injection
Therapeutic category: – Antiemetic, Anti Vomiting
Ondansetron Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Aqueous Solution in glass ampoules or vials.
Active Ingredient Concentration Total Content & Format Ondansetron (as HCl Dihydrate) 2 mg / ml 4 mg in 2 ml Glass Ampoule Ondansetron (as HCl Dihydrate) 2 mg / ml 8 mg in 4 ml Glass Ampoule Excipients Citric Acid / Sodium Citrate pH Buffer System (pH 3.3 to 4.0) *Pack Sizes: Tray of 5/10 Ampoules or Box of 50 Ampoules.
Ondansetron Orally Disintegrating Tablets
FreeProduct Composition & Available Formats
We supply Ondansetron ODT in the two primary compendial configurations required to support initial introductory pediatric dosing up to high-potency surgical and oncological maintenance regimens.
Active Ingredient Monograph Available Strengths Formulation Delivery Matrix Primary Clinical Application Ondansetron Base / Hydrochloride USP / BP / IP 4 mg Fast-Dispersing Hydrophilic Matrix (ODT) Pediatric & General Antiemetic: First-line baseline dosing for acute gastroenteritis, pediatric oncology protocols, and mild post-operative nausea. Ondansetron Base / Hydrochloride USP / BP / IP 8 mg Fast-Dispersing Hydrophilic Matrix (ODT) High-Potency Emetic Control: Advanced strength engineered for highly emetogenic chemotherapy cycles, abdominal radiation protocols, and immediate post-surgical recovery fields. Ondansetron Tablet
FreeProduct Composition & Available Strengths
We supply this critical supportive therapeutic in standard, internationally recognized strengths designed for exact preventative and rescue dosing.
Active Ingredient Available Strengths Primary Clinical Target Ondansetron HCl IP / BP / USP 4 mg Standard Prophylaxis: For moderate emetogenic chemotherapy, general post-operative rescue, and pediatric care. Ondansetron HCl IP / BP / USP 8 mg High-Potency Protection: For highly emetogenic cisplatin-based cancer regimens and severe surgical recovery. Ondansitron Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Flash-Dispersion ODT or Standard Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant peelable Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic ODT matrix.
Active Ingredient Strength Primary Clinical Function Ondansetron (as HCl Dihydrate) Ph.Eur./USP 4 mg (ODT / FCT) Pediatric & PONV Standard: Base therapeutic unit for post-operative nausea, severe pediatric gastroenteritis, and mild emetic triggers. Ondansetron (as HCl Dihydrate) Ph.Eur./USP 8 mg (ODT / FCT) Global Oncology Standard: High-dose adult maintenance therapy for highly emetogenic chemotherapy (CINV) and radiation therapy (RINV). Excipients (ODT Formulation) Mannitol / Crospovidone / Aspartame / Colloidal Silicon Dioxide / Premium Mint Flavoring Lyophilized Matrix / Superdisintegrant / Sweetener / Saliva-Stimulating Flavor (Engineered specifically to draw saliva into the tablet matrix, forcing a violent, sub-5-second structural collapse on the tongue without a bitter aftertaste) *Pack Sizes: 10×10 Peelable Alu-Alu Blisters (Optimized specifically for strict oncology and surgical dispensing regimens).
Oral Rehydration Salts (Sachets)
FreeProduct Composition & Osmolarity Calibration
We manufacture the exact Low-Osmolarity ORS configuration, which has been clinically proven to reduce stool volume, eliminate the need for intravenous infusions by greater than 33%, and physically shorten recovery windows compared to old high-osmolarity variants.
1. Powder Weight per Sachet (To Make 1 Litre of Solution)
Active Ingredient Mass per Sachet (Grams) Primary Physiological Function Glucose (Anhydrous) IP / BP / USP 13.50 g The Driver: Drives the active sodium transport mechanism. Sodium Chloride IP / BP / USP 2.60 g The Replenisher: Replaces lost extracellular fluid ions. Trisodium Citrate Dihydrate IP/BP/USP 2.90 g The Buffer: Corrects systemic metabolic acidosis. Potassium Chloride IP / BP / USP 1.50 g The Balancer: Prevents systemic hypokalemia. Total Weight 20.50 g Standard sachet yield for exactly 1000 mL of water. Orciprenaline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly soluble sulphate salt.
Active Ingredient Strength Primary Clinical Function Orciprenaline Sulphate BP/Ph.Eur. 10 mg Pediatric / Initiation Standard: Base therapeutic unit for pediatric asthma management and dose titration. Orciprenaline Sulphate BP/Ph.Eur. 20 mg Global Adult Standard: Maximum adult maintenance dose for severe, chronic obstructive pulmonary disease (COPD). Excipients Microcrystalline Cellulose / Lactose Monohydrate / Maize Starch / Magnesium Stearate / Colloidal Silicon Dioxide Diluent / Binder / Disintegrant / Lubricant (Engineered specifically for rapid gastric dissolution and fast systemic absorption, providing relief within 30 minutes of oral administration) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-turnover acute dispensing and massive government health tenders).
Orlicure
FreeOrlicure is a pharmaceutical medication primarily containing Orlistat (120 mg) as its active ingredient. It is used for the management of obesity and weight loss by blocking the absorption of dietary fats in the intestines
Orligal
FreeOrligal capsules are anti-obesity medications used for weight loss and management. They primarily contain Orlistat as the active ingredient, typically in a 120 mg strength.
Orlistat Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Micro-Pellet Capsule or Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute chemical stability of the highly delicate API.
Active Ingredient Strength Primary Clinical Function Orlistat INN/Ph.Eur. 60 mg OTC / Retail Standard: Base therapeutic unit approved in many regions for over-the-counter (OTC) weight loss management in overweight adults. Orlistat INN/Ph.Eur. 120 mg Global Clinical Standard: Prescription-strength adult maintenance dose for clinical obesity (BMI > 30) and severe metabolic syndrome. Excipients (Capsule Pellets) Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Povidone / Talc Diluent / Superdisintegrant / Wetting Surfactant / Binder (Engineered specifically to maximize the dispersion of the API across the entire gastrointestinal lumen to maximize enzyme binding) *Pack Sizes: Bottles of 84/120 or 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic bariatric dispensing regimens, taken with every major meal).
Ornidazole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or Alu-PVC blister strips to ensure the absolute chemical stability of the highly photolabile active ingredient.
Active Ingredient Strength Primary Clinical Function Ornidazole INN/Ph.Eur. 500 mg Global Clinical Standard: Base therapeutic unit for the rapid eradication of protozoal and anaerobic pathogens. Excipients Microcrystalline Cellulose / Maize Starch / Sodium Starch Glycolate / Hypromellose / Titanium Dioxide Diluent / Binder / Superdisintegrant / Premium Film-Coating (Engineered specifically to create an impenetrable barrier that completely masks the notoriously bitter, foul taste of the nitroimidazole API, ensuring flawless patient compliance) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 3-to-10 day acute anti-infective dispensing regimens).
ORS – Oral Rehydration Salt
FreeOral Rehydration Salts IP
Each 4.2 gm contains :
Sodium Chloride IP 0.52 gm
Potassium Chloride IP 0.30 gm
Sodium Citrate IP 0.58 gm
Anhydrous Glucose IP 2.70 gm
Excipients qs
Refreshing FlavourOral Rehydration Salts IP
Each 21 gm contains :
Sodium Chloride IP 2.6 gm
Potassium Chloride IP 1.5 gm
Sodium Citrate IP 2.9 gm
Anhydrous Dextrose IP 13.5 gm
Excipients qs
Refreshing Orange FlavourOral Rehydration Salts BP
Each 4.2 gm contains :
Sodium Chloride BP 0.52 gm
Potassium Chloride BP 0.30 gm
Sodium Citrate BP 0.58 gm
Anhydrous Glucose BP 2.70 gm
Refreshing FlavourOral Rehydration Salts BP
Each 21 gm contains :
Sodium Chloride BP 2.6 gm
Potassium Chloride BP 1.5 gm
Sodium Citrate BP 2.9 gm
Anhydrous Glucose BP 13.5 gm
Refreshing Orange FlavourORASEL / ORAL REHYDRATION SALT B.P. Each 21 gm sachet contains: Anhydrous glucose BP 13.5 g Sodium Chloride BP 2.6 g Sodium citrate BP 2.9 g Potassium Chloride BP 1.5 g Refreshing orange Flavour
HEALTHY ORS /ORAL REHYDRATION SALTS BP EACH 20.5 GM CONTAINS:: – POTASSIUM CHLORIDE BP 1.5 GM
– SODIUM CITRATE BP 2.9 GM
– ANHYDROUS GLUCOSE BP 13.5 GM
– SODIUM CHLORIDE BP BP 2.6 GM – EXCIPIENTS QSUsage: – To replace salts and water that the body loses when you have dehydration caused by gastroenteritis, diarrhea, or vomiting
Category: – Generic Drugs and Medicine
Therapeutic category: – Generic Drugs
Oseltamivir Tablet
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Hard Gelatin Capsule, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the hygroscopic phosphate salt.
Active Ingredient Strength Primary Clinical Function Oseltamivir Phosphate USP/Ph.Eur. 75 mg (Equivalent to Oseltamivir free base) Global Standard: Target adult dose for rapid treatment and prophylaxis of Influenza A/B. Excipients Pregelatinized Starch / Croscarmellose Sodium / Povidone / Sodium Stearyl Fumarate Diluent / Superdisintegrant (Engineered for immediate gastric capsule rupture and rapid systemic absorption) *Pack Sizes: 1×10 Blisters (Optimized perfectly for the standard 5-day acute treatment regimen of two capsules daily).
Oxacillin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Crystalline Powder buffered for stability in glass vials.
Active Ingredient Strength Sodium Content Oxacillin Sodium USP/BP 500 mg Approx. 1.4 mEq (32 mg) Oxacillin Sodium USP/BP 1000 mg (1 g) Approx. 2.8 mEq (64 mg) Oxacillin Sodium USP/BP 2000 mg (2 g) High-Dose Protocols Buffer Dibasic Sodium Phosphate Maintains pH upon reconstitution *Pack Sizes: Single Vial or Tray of 10/50 Vials. (Requires reconstitution with Sterile Water for Injection).
Oxaliplatin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Aqueous Concentrate in glass vials. (Also available as Lyophilized Powder depending on market preference).
Active Ingredient Strength Volume Oxaliplatin USP/BP 5 mg / ml 10 ml Vial (Total 50 mg) Oxaliplatin USP/BP 5 mg / ml 20 ml Vial (Total 100 mg) Excipients Water for Injection Preservative-Free Solution *Pack Sizes: Single Vial. (Must be handled with strict cytotoxic precautions).
Oxcarbazepine Tablet
FreeProduct Composition & Available Strengths
We manufacture Oxcarbazepine in the full, internationally standardized range of strengths to allow for the precise, progressive dose titration mandatory in anti-epileptic therapy.
Active Ingredient Available Strengths Primary Clinical Target Oxcarbazepine IP / BP / USP 150 mg Pediatric & Initial Titration: For low-dose introductory phases to assess patient tolerance. Oxcarbazepine IP / BP / USP 300 mg Standard Maintenance: The foundational daily maintenance dose for adolescent and adult stabilization. Oxcarbazepine IP / BP / USP 600 mg High-Potency Control: For refractory focal seizures or high-threshold therapeutic stabilization. Oxybutynin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Polymeric Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE desiccant bottles to ensure the absolute chemical stability of the controlled-release hydrogel network.
Active Ingredient Strength Primary Clinical Function Oxybutynin Chloride USP/Ph.Eur. 5 mg (ER) Initiation Standard: Base once-daily titration unit for the gradual introduction of antimuscarinic therapy. Oxybutynin Chloride USP/Ph.Eur. 10 mg / 15 mg (ER) Global Clinical Standard: Advanced maintenance doses for severe, refractory Overactive Bladder and neurogenic detrusor overactivity. Excipients Hypromellose (HPMC) / Lactose Anhydrous / Macrogol (PEG) / Magnesium Stearate / Titanium Dioxide Hydrophilic Polymer Matrix / Diluent / Plasticizer / Premium Film-Coating (Engineered specifically to form a highly viscous external gel barrier upon swallowing, controlling the exact 24-hour drug diffusion rate) *Pack Sizes: Bottles of 30 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-compliance 30-day chronic urology dispensing regimens).
Oxytetracycline injection
FreeComposition
Each ml Contains :
Oxytetracycline Hcl I.P. …….. 50 mg
Lidocain U.S.P. ……………… 2 %
Water for Injection I.P. Q.S. 30 mlUsage: – used in medicine to treat various bacterial infections
Category: – antibiotic injection
Therapeutic category: – antibiotic
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Oxytetracycline Veterinary injection
FreeComposition
Oxytetracycline 5% 100 ML vet INJ
Oxytetracycline 5% 30 ML vet INJ
Oxytetracycline 20% (LA) 50 vet ML
Usage: – used in veterinary medicine to treat various 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
Pancreatin & L-Ornithine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the biological proteins and the highly hygroscopic amino acid.
Active Ingredient Strength Primary Clinical Function Pancreatin (Porcine Origin) Ph.Eur./USP 170 mg
(Standardized Lipase/Protease/Amylase)Gastrointestinal Standard: Intraluminal enzymatic digestion of complex macronutrients to reverse malabsorption. L-Ornithine (as L-Ornithine L-Aspartate / LOLA) 150 mg Hepatology Standard: Hepatic urea cycle activation for aggressive ammonia detoxification and liver regeneration. Excipients Methacrylic Acid Copolymer / Microcrystalline Cellulose / Crospovidone / Magnesium Stearate Enteric Barrier Coating (for Pancreatin) / Diluent / Superdisintegrant (Engineered specifically to separate the amino acid from the enzymes and ensure targeted duodenal release of the biologicals) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-compliance chronic hepato-gastro dispensing regimens).
Pancreatin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Enteric-Coated Tablet or Hard Capsule (containing Enteric Minimicrospheres), packed exclusively in highly secure, moisture-resistant Alu-Alu blisters or desiccant-lined HDPE bottles to ensure the absolute stability of the biological proteins.
Active Ingredient Strength (Standardized USP Units) Primary Clinical Function Pancreatin (Porcine Origin) Ph.Eur./USP 10,000 Lipase Units
(approx. 33,200 Protease / 33,200 Amylase)Pediatric / Initiation Standard: Base therapeutic unit for pediatric Cystic Fibrosis patients and meal-snack titration. Pancreatin (Porcine Origin) Ph.Eur./USP 25,000 Lipase Units
(approx. 85,000 Protease / 74,700 Amylase)Global Clinical Standard: High-dose adult maintenance therapy for severe Exocrine Pancreatic Insufficiency and Pancreatectomy. Excipients Methacrylic Acid Copolymer / Macrogol / Simethicone / Microcrystalline Cellulose / Triethyl Citrate Enteric Barrier Coating / Plasticizer / Anti-Foaming Agent / Diluent (Engineered specifically to protect the biological extract from gastric acid and ensure rapid, synchronized dissolution in the duodenum) *Pack Sizes: Bottles of 100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-volume daily dispensing where patients may consume 3 to 10 units daily with every meal and snack).
Panthenol & Crude veterinary injection
FreeComposion
Panthenol Choline Chloride & Crude Liver VET INJ. 100 ML
Usage: –Injections of choline chloride may be used in veterinary medicine
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
Pantoprazole injection
FreeComposition
Pantoprazole Sodium 40 mg IV (VIAL) Vial
Usage: – Heartburn, acid reflux and gastro-esophageal reflux disease
Category: – Antacid & Anti ulcer drugs
Therapeutic category: – Antiulcer, Antacid
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
Pantoprazole & Domperidone Capsules
FreePantoprazole and domperidone capsules are combination medications used to treat gastrointestinal conditions involving both excess acid and motility issues, such as GERD and peptic ulcers. They are most commonly available in a fixed-dose strength of 40 mg pantoprazole and 30 mg domperidone.
Pantoprazole & Domperidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Dual-Release Capsule or Bilayer Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly acid-labile Pantoprazole and the SR polymer network.
Active Ingredient Strength Primary Clinical Function Pantoprazole Sodium Sesquihydrate USP/Ph.Eur. 40 mg (Enteric-Coated) Global Clinical Standard: Profound, 24-hour suppression of gastric acid production. Domperidone Maleate BP/Ph.Eur. 30 mg (Sustained-Release) Continuous 24-hour peripheral prokinetic action to accelerate gastric emptying and prevent nausea. Excipients Methacrylic Acid Copolymer / Hypromellose (HPMC) / Mannitol / Magnesium Stearate Enteric Barrier Coating / Hydrophilic SR Polymer Matrix / Diluent (Engineered specifically to perfectly isolate the two APIs and control their entirely separate intestinal dissolution rates) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-compliance 14-to-28 day chronic gastroenterology dispensing regimens).
Pantoprazole And Levosulpiride Capsules
FreePantoprazole and levosulpiride capsules are a combination therapy used for gastrointestinal conditions where excess acid is accompanied by motility issues. They are most commonly available in a fixed-dose strength of 40 mg (enteric-coated) and 75 mg (sustained-release).Pantoprazole Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Off-White Cake) in clear glass vials.
Active Ingredient Strength Reconstitution Requirement Pantoprazole Sodium USP/BP 40 mg Requires 10 ml of 0.9% Sodium Chloride Excipients Sodium Hydroxide / Edetate Disodium Alkalizing Agent / Stabilizer *Pack Sizes: Single Vial or Tray of 10 Vials. (Often packed with a 10 ml ampoule of 0.9% NaCl diluent).
Pantoprazole Tablets
FreePantoprazole Tablets IP 40 mg
Each Enteric Coated tablet contains
Pantoprazole Sodium IP
Eq. To Pantoprazole 40 mgPenta-20
Pantoprazole Tablets 20 mg
Each Enteric Coated Tablet Contains
Pantoprazole Sodium Sesquihydrate
Eq To Pantoprazole 20 mgPenta – 40
Pantoprazole Tablets 40 mg
Each Entreric Coated tablet contains
Pantoprazole Sodium Sesquihydrate
Eq. To pantoprazole 40 mgUsage: – Heartburn, acid reflux and gastro-esophageal reflux disease
Category: – Antacid & Anti ulcer drugs
Therapeutic category: – Antiulcer, Antacid
Paracetamol & Caffeine Anhydrous Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets or Uncoated Tablets. The anhydrous caffeine allows for a harder, more durable tablet suitable for bulk transport.
Active Ingredient Strength (Standard) Strength (Extra Power) Technical Grade Paracetamol IP/BP/USP 500 mg 650 mg Micronized Caffeine Anhydrous IP/BP/USP 30 mg 50 mg / 65 mg Moisture Content < 0.5% Excipients Q.S. Starch / PVP K-30 Binder Paracetamol & caffeine tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Uncoated Tablets in blister packs. Multiple strength combinations are available.
Product Variant Paracetamol Content Caffeine (Anhydrous) Common Name Standard Extra 500 mg 30 mg Panadol Extra Generic High Caffeine 500 mg 65 mg Migraine Relief Forte Strength 650 mg 50 mg Extra Strength Paracetamol & Diclofenac Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White, Orange, or Red). The coating is non-enteric to ensure immediate disintegration.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/USP 325 mg / 500 mg Central Analgesic Diclofenac Potassium IP/USP 50 mg Rapid Anti-Inflammatory Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Binder / Super-Disintegrant Paracetamol & Diclofenac Sodium Tablets
FreeProduct Composition & Strength
We supply this product as Enteric Coated or Film Coated Tablets in blister packs.
Active Ingredient Strength (Standard) Role Diclofenac Sodium IP/BP/USP 50 mg Anti-inflammatory / Analgesic Paracetamol IP/BP/USP 500 mg Analgesic / Antipyretic Excipients Q.S. Binder / Disintegrant Paracetamol & Orphenadrine Citrate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets in blister packs. We offer both Standard and Forte strengths.
Product Variant Paracetamol Content Orphenadrine Citrate Common Name Standard Strength 450 mg 35 mg Norgesic Generic Forte Strength 650 mg 50 mg Norgesic Forte Generic Excipients Q.S. — Binder / Filler Paracetamol Caffeine Chlorpheniramine Maleate Phenylephrine Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) optimized for maximum clinical efficacy.
Active Ingredient Strength (per Tablet) Primary Clinical Function Paracetamol (Acetaminophen) 325 mg / 500 mg The Pain & Fever Reliever: Targets aches and chills. Caffeine (Anhydrous) 30 mg The Potentiator: Boosts pain relief and alertness. Chlorpheniramine Maleate 2 mg / 4 mg The Antiallergic: Stops sneezing and runny nose. Phenylephrine HCl 5 mg / 10 mg The Decongestant: Clears blocked sinuses. paracetamol caffeine phenylephrine cpm Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (often colored/shaped for brand differentiation). This is a “fixed-dose combination” optimized for adult efficacy.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 500 mg Fever & Pain Reducer Caffeine (Anhydrous) 30 mg Analgesic Booster / Alertness Phenylephrine HCl 5 mg / 10 mg Nasal Decongestant Chlorpheniramine Maleate 2 mg / 4 mg Antiallergic Paracetamol Diclo Sodium Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated or Enteric Coated Tablets (typically White, Orange, or Yellow). The coating protects the stomach from the direct irritation of Diclofenac.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/USP 500 mg / 325 mg Central Analgesic / Antipyretic Diclofenac Sodium IP/USP 50 mg Peripheral Anti-Inflammatory Excipients Q.S. Maize Starch / Magnesium Stearate / Talc Binder / Lubricant Paracetamol Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Iso-osmotic Solution ready for direct intravenous infusion.
Active Ingredient Concentration Total Content & Format Paracetamol BP/USP 10 mg / ml 1000 mg (1 g) in 100 ml Glass Bottle / FFS Plastic Bottle Paracetamol BP/USP 150 mg / ml 300 mg in 2 ml Glass Ampoule (IM/IV use) Excipients Mannitol / Cysteine Hydrochloride Isotonic Agent / Oxygen Scavenger (Antioxidant) *Pack Sizes: 100 ml Single Bottle or Box of 10 Ampoules.
Paracetamol injection
FreeProduct Composition & Strength
We supply this product as a ready-to-use infusion in glass bottles or IV bags.
Active Ingredient Strength Total Content Paracetamol IP/USP 10 mg / ml 1000 mg / 100 ml *Supplied in 100ml Glass Bottles or FFS (Form-Fill-Seal) Plastic Bottles.
Paracetamol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Standard) or Film Coated/Caplets (Easy Swallow). We offer varying release profiles.
Active Ingredient Strength (Standard) Role Paracetamol IP/BP/USP 500 mg Global Standard Adult Dose Paracetamol IP/BP/USP 650 mg High Potency / Sustained Pain Paracetamol IP/BP/USP 1000 mg (ER) Extended Release (Osteoarthritis) Excipients Q.S. Starch (Binder) / Lubricant Paracetamol Tablets
FreeParacetamol Tablets IP
Each Uncoated tablet contains :
Paracetamol IP 500 mgParacetamol Tablets IP 650 mg
Each uncoated Tablet Contains:
Paracetamol IP 650 mg
Excipients – QSParacetamol Tablets BP
Each Uncoated tablet contains :
Paractamol BP 100 mgParacetamol Tablets BP
Each Uncoated tablet contains :
Paracetamol BP 250 mgParafen te
Paracetamol with Ibuprofen Tablets
Each Uncoated tablet contains :
Ibuprofen IP 400 mg
Paracetamol IP 325 mgPARACETAMOL AND CAFFEINE TABLETS
Each uncoated Tablets Contains:
Paracetamol BP 325 mg
Caffeine anhydrous BP 30 mg
Excipients – QSParacetamol and Orphenadrine Citrate Tablets
Each uncoated tablet contains:
Orphenadrine citrate 35 mg
Paracetamol 450 mg
Excipients – QS
Each Uncoated Caplet contains :
Paracetamol BP 500 mg
Caffeine Anhydrous BP 30 mgPARACETAMOL AND CAFFEINE
Each uncoated Tablet contains:
Paracetamol BP 325 mg
Caffeine BP 30 mg
q.s. –PARACETAMOL,CAFFEINE,PHENYLEPHRINE HCL AND CHOLRPHENIRAMINE MALEATE TABLETS
Each Uncoated Tablet Contains:
Paracetamol BP 325 mg
Caffeine BP 30 mg
Chlorpheniramine maleate BP 2 mg
Phenylephrine Hcl BP 2.5 mg
Colour : Sunset Yellow –
Excipients – QSPARACETAMOL,CAFFEINE,PHENYLEPHRINE AND CHLORPHENIRAMINE TABLETS
Each uncoated Tablet contains:
Paracetamol BP 325 mg
Caffeine BP 15 mg
Phenylephrine BP 2.5 mg
Chlorpheniramine BP 2 mg
Tartrazine In House –Usage: – Treat aches and pain
Category: – Anti Analgesic Painkiller Drugs
Therapeutic category: – NSAID, Analgesic, Antipyretic, Anti Inflammatory
Paracetamol, Caffeine & Phenylephrine Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Film Coated Tablets. The absence of an antihistamine makes this the ideal “Work-Safe” cold remedy.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 500 mg / 650 mg Fever & Pain Reducer Caffeine Anhydrous IP/BP/USP 30 mg Alertness / Analgesic Booster Phenylephrine HCl IP/BP/USP 5 mg / 10 mg Nasal Decongestant Excipients Q.S. Povidone / Starch / MCC Paracetamol, Caffeine, Phenylephrine HCl & CPM Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets or Film Coated Tablets (often colored Red, Blue, or Bi-layered). The formulation is balanced for adult physiology.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 500 mg Fever & Pain Reducer Caffeine Anhydrous IP/BP/USP 30 mg Analgesic Potentiator / Alertness Phenylephrine HCl IP/BP/USP 5 mg / 10 mg Nasal Decongestant Chlorpheniramine Maleate IP/BP/USP 2 mg / 4 mg Antiallergic / Antihistamine Excipients Q.S. Starch / MCC / Colorants Paracetamol, Diclofenac Potassium & Caffeine Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (often capsule-shaped). The coating masks the bitter taste of Caffeine and the astringency of Diclofenac.
Active Ingredient Strength (Standard) Therapeutic Role Paracetamol IP/BP/USP 325 mg / 500 mg Central Analgesic / Antipyretic Diclofenac Potassium BP/USP 50 mg Rapid Anti-Inflammatory Caffeine Anhydrous BP/USP 30 mg Adjuvant / Vasoconstrictor Excipients Q.S. Microcrystalline Cellulose / HPMC Paracetamol, Diclofenac Sodium & Caffeine Tablets
FreeProduct Composition & Standard Strengths
We supply this product in standardized Fixed-Dose Combinations (FDCs) designed for maximum therapeutic synergy.
Paroxetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Polymeric Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the extended-release hydrogel network.
Active Ingredient Strength Primary Clinical Function Paroxetine (as HCl Hemihydrate) Ph.Eur./USP 12.5 mg (CR) Initiation Standard: Base titration unit to safely acclimatize the brain and minimize initial side effects. Gold standard for PMDD. Paroxetine (as HCl Hemihydrate) Ph.Eur./USP 25 mg (CR) Global Clinical Standard: Standard adult maintenance dose for Major Depressive Disorder and Severe Panic Disorder. Paroxetine (as HCl Hemihydrate) Ph.Eur./USP 37.5 mg (CR) Advanced Psychiatric Standard: High-dose maintenance therapy for treatment-resistant depression and refractory anxiety. Excipients Hypromellose (HPMC) / Methacrylic Acid Copolymer / Lactose Monohydrate / Magnesium Stearate / Triethyl Citrate Hydrophilic SR Polymer Matrix / Enteric Coating / Diluent / Plasticizer (Engineered to absolutely block stomach acid and control the exact 24-hour intestinal diffusion rate) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic psychiatric dispensing regimens).
Pazopanib Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered, High-Density Film-Coated Tablet, packed exclusively in highly secure, child-resistant heavy-gauge HDPE bottles or specialized Alu-Alu blister strips to ensure the absolute chemical stability of the cytotoxic molecule and prevent accidental exposure.
Active Ingredient Strength Primary Clinical Function Pazopanib HCl INN/Ph.Eur. 200 mg (Base Equivalent) Dose-Modification Standard: Essential unit for precise dose reduction in patients experiencing severe hepatic toxicity or adverse drug reactions. Pazopanib HCl INN/Ph.Eur. 400 mg (Base Equivalent) Global Clinical Standard: Primary therapeutic unit designed to achieve the massive 800 mg daily protocol with minimal pill burden. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone K30 / Magnesium Stearate / Hypromellose / Titanium Dioxide Diluent / Superdisintegrant / Binder / Lubricant / Premium Cytotoxic-Barrier Film-Coating (Engineered specifically to seal the lethal HPAPI inside the tablet, completely protecting healthcare workers and caregivers from highly toxic dust exposure) *Pack Sizes: Bottles of 30 or 60 Tablets (Optimized specifically for strict 30-day chronic oncology dispensing regimens).
Pemetrexed Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Light-Yellow Cake) in glass vials.
Active Ingredient Strength Reconstitution Pemetrexed Disodium 100 mg Requires 0.9% Sodium Chloride Pemetrexed Disodium 500 mg Requires 0.9% Sodium Chloride Pemetrexed Disodium 1000 mg (1 g) High-Dose Protocols Excipients Mannitol / Hydrochloric Acid / Sodium Hydroxide Bulking Agent / pH Adjusters (pH 6.6 – 7.8) *Pack Sizes: Single Vial. (Must be handled with strict cytotoxic precautions).
Pentoxifylline Tablets
FreePentoxifylline Tablets 400 mg
Each Filmcoated tablet contains :
Pentoxifylline BP 400 mgUsage: – To reduce leg pain caused by poor blood circulation
Category: – Anti Cardiovascular drugs
Therapeutic category: – Cardiovascular
Perindopril Erbumine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips equipped with active desiccants to ensure the absolute chemical stability of the highly degradable Erbumine salt.
Active Ingredient Strength Primary Clinical Function Perindopril Erbumine Ph.Eur./USP 2 mg Initiation Standard: Base titration dose for elderly patients or those with severe heart failure/renal impairment to prevent sudden hypotension. Perindopril Erbumine Ph.Eur./USP 4 mg Hypertension Standard: Standard adult maintenance dose for the continuous control of essential hypertension. Perindopril Erbumine Ph.Eur./USP 8 mg Cardiovascular Risk Standard: Maximum maintenance dose for profound risk reduction in patients with stable coronary artery disease. Excipients Microcrystalline Cellulose / Lactose Anhydrous / Hydrophobic Colloidal Silica / Magnesium Stearate Diluent / Alkaline Stabilizer / Moisture Scavenger / Lubricant (Engineered specifically to create a hyper-dry internal tablet matrix that absolutely prevents hydrolytic cyclization of the API) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict 30-day chronic cardiology dispensing regimens).
Phenazopyridine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant PVC/PVDC or Alu-PVC blister strips to ensure the stability of the active dye compound.
Active Ingredient Strength Primary Clinical Function Phenazopyridine Hydrochloride USP/Ph.Eur. 100 mg Standard OTC/Initiation dose for mild-to-moderate urinary tract discomfort. Phenazopyridine Hydrochloride USP/Ph.Eur. 200 mg Global Prescription Standard: Maximum adult dose for severe dysuria and post-operative catheter trauma. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate Diluent / Superdisintegrant (Engineered for rapid gastric dissolution and swift renal clearance) Phenazopyridine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant high-density PVC/PVDC or Alu-PVC blister strips to ensure absolute chemical stability and prevent dye leakage.
Active Ingredient Strength Primary Clinical Function Phenazopyridine HCl USP/Ph.Eur. 100 mg OTC Standard: Base therapeutic unit for mild to moderate UTI symptom relief. Phenazopyridine HCl USP/Ph.Eur. 200 mg Prescription Standard: Maximum adult dose for severe, acute dysuria and post-surgical trauma. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Magnesium Stearate / Heavy Carnauba Wax Coating Diluent / Superdisintegrant / Binder / Lubricant / Premium Film-Coating (Engineered specifically to seal the intense red dye inside the tablet, preventing it from staining the patient’s hands or mouth upon swallowing) *Pack Sizes: 10×10 Blisters (Optimized specifically for high-turnover acute dispensing and short-term 2-day urology protocols).
Pheniramine Maleate Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Clear Solution in glass ampoules.
Active Ingredient Strength Total Content (2 ml) Pheniramine Maleate BP/USP 22.75 mg / ml 45.5 mg (per 2 ml Ampoule) Excipients Water for Injection Isotonic Solution *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
PHENIRAMINE MALEATE INJECTION
FreeComposition
Each ml. contains: Pheniramine Maleate I.P. 22.75 mg.
Methyl Paraben I.P. 0.135 % w/v (As Preserva9ve)
Propyl Paraben I.P. 0.015% w/v (As Preserva9ve)
Water for Injec9on I.P. Q.SUsage: – It is used to relieve pruritus (itching) associated with various dermatological conditions.
Category: –Pheniramine Maleate injection
Therapeutic category: – Pheniramine Maleate injection
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
Pheniramine Maleate Tablets
FreePheniramine Maleate Tablets IP 25 mg
Each Uncoated Tablet Contains :
Pheniramine Maleate IP 25 mgPheniramine Maleate veterinary injection
FreeComposition
Pheniramine Maleate VET INJ. 30 ML
Usage: – It is used to relieve pruritus (itching) associated with various dermatological conditions.
Category: –Pheniramine Maleate injection
Therapeutic category: – Pheniramine Maleate injection
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
Phenobarbital Tablets
FreePhenobarbitone Tablets IP
Each Uncoated tablet contains :
Phenobarbitone IP 30 mg
Excipients q.sPhenobarbitone Tablets IP 60 mg
Phenobarbital Tablets IP 60 mg
Each Uncoated tablet contains :
Phenobarbitone IP 60 mg
Phenobarbital
Excipients q.sPhenobarbital Tablets BP
Each Uncoated tablet contains :
Phenobarbital BP 30 mgPhenobarbital Tablets BP 60 mg
Each Uncoated tablet contains :
Phenobarbital BP 60 mg Excipients q.sPHENOBARBITAL TABLETS BP 90 MG Each Uncoated tablet contains : Phenobarbital BP 90 mg
Excioients 0 QSPhenobarbital Tablets BP 100 mg
Each Uncoated tablet contains :
Phenobarbital BP 100 mg Excipients -QSUsage: – To control seizures
Category: – Anti Hypertensive / Cardiac Drugs
Therapeutic category: – Hypertensive
Phenyl Butazone & Sodium Salicylate veterinary injection
FreeComposition
Phenyl Butazone & Sodium Salicylate VET INJ. 30 ML
Phenyl Butazone & Sodium Salicylate VET INJ. 100 ML
Usage: – Usage in Veterinary Medicine: Phenylbutazone is frequently employed in horses, dogs, and other large animals.
Category: – veterinary injection
Therapeutic category: – veterinarian’s assessment
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
Phenytoin Tablets
FreePhenytoin Sodium tablets IP
Each Sugarcoated tablet contains :
Phenytoin Sodium IP 100 mgPhenytoin Sodium Tablets IP 100 mg
Each Filmcoated Tablets Contains:
Phenytoin Sodium IP 100 mgPhenytoin Tablets BP
Each Sugar Coated tablet contains :
Phenytoin Sodium 25 mgPhenytoin Sodium Tablets BP
Each Sugar Coated tablet contains :
Phenytoin Sodium BP 100 mgUsage: – Treat epilepsy
Category: – Anti Hypertensive / Cardiac Drugs
Therapeutic category: – Anticonvulsant, Antiepileptic
Phytomenadione Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Aqueous Colloidal Solution or Mixed-Micelle Emulsion in glass ampoules.
Active Ingredient Strength Primary Indication Phytomenadione BP/USP 1 mg / 0.5 ml Pediatric: Prophylaxis of HDN Phytomenadione BP/USP 10 mg / 1 ml Adult: Anticoagulant Overdose / Bleeding Excipients Lecithin / Glycocholic Acid (or Cremophor) Solubilizer (Mixed-Micelle system) *Pack Sizes: Tray of 10 Ampoules or 100 Ampoules.
Phytomenadione Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Opaque Coated Tablet, packed exclusively in highly secure, moisture-resistant, and entirely light-blocking Alu-Alu or Opaque PVC/PVDC blister strips to ensure the absolute chemical stability of the photosensitive vitamin.
Active Ingredient Strength Primary Clinical Function Phytomenadione (Vitamin K1) BP/USP 10 mg Global Clinical Standard: Base therapeutic unit for the predictable reduction of elevated INR and treatment of hypoprothrombinemia. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Colloidal Silicon Dioxide / Magnesium Stearate / Titanium Dioxide Diluent / Binder / Glidant / Lubricant / Heavy Opaque Film-Coating (Engineered specifically to form an impenetrable barrier against ultraviolet and visible light degradation) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-turnover pharmacy dispensing and cardiology ward stockpiles).
Pioglitazone Tablets
FreePioglitazone Tablets IP 15 mg
Each Uncoated tablet contains :
Pioglitazone Hydrochloride IP
Eq. To Pioglitazone 15 mgPioglitazone Tablets IP 30 mg
Each Uncoated tablet contains :
Pioglitazone Hydrochloride IP
Eq. To Pioglitazone 30 mgPioglitazone With Metformin Tablet
Each Film Coated Tablet contains :
Pioglitazone Hydrochloride IP
Eq. to Pioglitazone 15 mg
Metformin Hydrochloride IP 500 mgUsage: – Type 2 diabetes mellitus
Category: – Anti Diabetic drugs
Therapeutic category: – Anti Diabetic
Piperacillin Sodium injection
FreeComposition
Piperacillin Sodium USP equivalent to
Piperacillin 4g + Tazobactam sodium equivalent to
Tazobactam 0.5mg injection
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
Piperacillin Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder buffered with Sodium Citrate/EDTA.
Strength (Ratio 8:1) Piperacillin Content Tazobactam Content 4.5 g (Standard Adult) 4000 mg (4 g) 500 mg (0.5 g) 2.25 g (Pediatric/Renal) 2000 mg (2 g) 250 mg (0.25 g) Sodium Content ~2.35 mEq per gram of Piperacillin Monitor in Heart Failure *Pack Sizes: Single Vial or Tray of 10 Vials.
Piracetam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Clear Solution in glass ampoules or large volume infusion bottles.
Active Ingredient Strength Volume Piracetam BP/USP 200 mg / ml 5 ml Ampoule (1 g Total) Piracetam BP/USP 200 mg / ml 15 ml Ampoule (3 g Total) Piracetam BP/USP 200 mg / ml 60 ml Infusion Bottle (12 g Total) Excipients Sodium Acetate / Acetic Acid Buffer (pH 5.0 – 7.0) *Pack Sizes: Tray of 5/10 Ampoules or Single Infusion Bottle.
Piracetam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or heavy-gauge PVC/PVDC blister strips to ensure the absolute chemical stability of the highly hygroscopic API.
Active Ingredient Strength Primary Clinical Function Piracetam Ph.Eur./USP 400 mg Initiation / Pediatric Standard: Base unit for pediatric dyslexia and mild vertigo management. Piracetam Ph.Eur./USP 800 mg Global Cognitive Standard: Standard adult maintenance dose for age-related cognitive decline and memory impairment. Piracetam Ph.Eur./USP 1200 mg Acute Neurology Standard: Massive-dose unit designed specifically for Cortical Myoclonus and intensive post-stroke rehabilitation protocols to minimize pill burden. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Macrogol (PEG) / Colloidal Silicon Dioxide / Magnesium Stearate High-Density Diluent / Superdisintegrant / Premium Film-Coating (Engineered specifically to compress the massive API load into a smooth, swallowable, moisture-resistant oblong tablet) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, high-volume chronic neurology dispensing where patients may consume 2.4g to 4.8g daily).
Piroxicam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile, Clear, Pale Yellow to Yellow Aqueous-Solvent Solution in glass ampoules.
Active Ingredient Concentration Total Content & Format Piroxicam USP/BP 20 mg / ml 20 mg in 1 ml Glass Ampoule Piroxicam USP/BP 20 mg / ml 40 mg in 2 ml Glass Ampoule Excipients Propylene Glycol / Benzyl Alcohol Solvent System / Local Anesthetic (Preservative) *Pack Sizes: Tray of 10 Ampoules, 50 Ampoules, or 100 Ampoules.
Piroxicam Injection
FreeComposition
Each mL contains: Piroxicam BP : 20 mg
Benzyl Alcohol BP (as preserva9ve) : 2 % v/v
Water For Injec9on BP : q.s 1mlUsage: –used to manage postoperative pain after certain surgical procedures.
Category: – piroxicam injection
Therapeutic category: – piroxicam injection
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
Piroxicam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet or Hard Gelatin Capsule, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly insoluble active ingredient.
Active Ingredient Strength Primary Clinical Function Piroxicam USP/Ph.Eur. 10 mg Initiation / Elderly Standard: Reduced dose for elderly patients or those with mild renal impairment to mitigate gastrointestinal risks. Piroxicam USP/Ph.Eur. 20 mg Global Clinical Standard: Maximum adult daily dose for the once-daily, continuous suppression of severe rheumatoid and osteoarthritis. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Sodium Lauryl Sulfate / Magnesium Stearate Diluent / Superdisintegrant / Wetting Agent / Lubricant (Engineered specifically with high-grade surfactants to force the rapid gastric dissolution of the highly water-insoluble Piroxicam API) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic rheumatology and orthopedic dispensing regimens).
