Unnati Pharmax

Asthalin Respules
Composition: Salbutamol Sulphate Inhalation Solution
International Trade Name: Ventolin®

Asthalin Respules is a high-quality Salbutamol inhalation solution, a trusted short-acting β2-agonist (SABA) equivalent to the internationally recognized Ventolin®. Manufactured in WHO-GMP certified facilities, Asthalin Respules supports effective acute and maintenance respiratory care programs for patients with asthma and chronic obstructive pulmonary disease (COPD).

Salbutamol works by stimulating β2-adrenergic receptors in bronchial smooth muscle, resulting in rapid bronchodilation and relief from bronchospasm, wheezing, and shortness of breath. Asthalin Respules are primarily indicated for treatment and prevention of bronchospasm in asthma, COPD, and other reversible obstructive airway diseases, and for use in acute exacerbations via nebulization.

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Asthalin Respules are manufactured under stringent GMP and respiratory-product quality standards, ensuring consistent dose delivery, safety, and stability. The respules are supplied in sterile, unit-dose, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, emergency care units, pulmonology clinics, and international pharmaceutical distributors.

Bilypsa 4 mg Tablets
Composition: Saroglitazar 4 mg
International Trade Name: Lipaglyn®

Bilypsa 4 mg is a high-quality Saroglitazar oral tablet, a trusted lipid-lowering and insulin-sensitizing therapy equivalent to the internationally recognized Lipaglyn®. Manufactured in WHO-GMP certified facilities, Bilypsa supports advanced metabolic disorder management, particularly in patients with diabetic dyslipidemia and hypertriglyceridemia.

Saroglitazar is a dual peroxisome proliferator-activated receptor (PPAR) α/γ agonist that works by reducing triglycerides, improving HDL cholesterol, and enhancing insulin sensitivity, thereby improving overall lipid and glucose metabolism. Bilypsa 4 mg Tablets are primarily indicated for management of diabetic dyslipidemia in type 2 diabetes mellitus patients and hypertriglyceridemia not controlled by statin therapy alone.

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Bilypsa 4 mg Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, endocrinology clinics, tertiary care centers, and international pharmaceutical distributors.

Testosign Gel 1% w/w
Composition: Testosterone Gel 1% w/w
International Trade Name: AndroGel®

Testosign Gel 1% is a high-quality transdermal testosterone replacement therapy, a trusted formulation equivalent to the internationally recognized AndroGel®. Manufactured in WHO-GMP certified facilities, Testosign Gel supports comprehensive androgen replacement programs in men with testosterone deficiency (hypogonadism).

Testosterone gel delivers physiological testosterone levels through transdermal absorption, helping restore and maintain normal serum testosterone concentrations, improve sexual function, energy levels, muscle mass, bone density, and overall well-being. Testosign Gel 1% is primarily indicated for replacement therapy in adult males with primary or secondary hypogonadism due to inadequate endogenous testosterone production.

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Testosign Gel 1% is manufactured under strict GMP and quality standards, ensuring consistent potency, safety, and long-term stability. The gel is supplied in secure, tamper-evident, export-grade packaging with complete regulatory documentation, making it suitable for endocrinology clinics, hospitals, specialty pharmacies, and international pharmaceutical distributors.

Diligan 25 mg Tablets
Composition: Meclizine Hydrochloride 25 mg
International Trade Name: Antivert® / Bonamine®

Diligan 25 mg is a high-quality Meclizine Hydrochloride oral tablet, a trusted antihistamine used for the prevention and treatment of motion sickness, vertigo, and associated nausea or vomiting. Manufactured in WHO-GMP certified facilities, Diligan supports effective vestibular disorder management and symptomatic relief of motion-induced discomfort.

Meclizine Hydrochloride works by blocking histamine H1 receptors in the central nervous system, reducing nausea, dizziness, and imbalance associated with motion sickness or vestibular disorders. Diligan 25 mg Tablets are primarily indicated for prevention and treatment of motion sickness, management of vertigo due to vestibular system dysfunction, and relief of associated nausea and vomiting.

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Diligan 25 mg Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, travel medicine centers, and international pharmaceutical distributors.

Pangraf 2 mg Capsules
Composition: Tacrolimus 2 mg
International Trade Name: Tacroz®

Pangraf 2 mg is a high-quality Tacrolimus oral capsule, a trusted immunosuppressant equivalent to the internationally recognized Tacroz®. Manufactured in WHO-GMP certified facilities, Pangraf supports advanced organ transplant programs and management of autoimmune disorders, helping prevent organ rejection and maintain graft function.

Tacrolimus is a calcineurin inhibitor that works by suppressing T-cell mediated immune responses, reducing the risk of transplant rejection and controlling autoimmune activity. Pangraf 2 mg Capsules are primarily indicated for prevention of organ rejection in kidney, liver, and heart transplant recipients, and management of severe autoimmune conditions like atopic dermatitis or ulcerative colitis in certain cases.

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Pangraf 2 mg Capsules are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, transplant centers, tertiary care hospitals, and international pharmaceutical distributors.

Optineuron Vitamin Injection
Composition: Multivitamins (B-Complex, Vitamin C, Vitamin E, and other essential vitamins)
International Trade Name: [Not Applicable / Custom Brand]

Optineuron is a high-quality multivitamin injection, designed to provide essential vitamins directly into the bloodstream for rapid absorption and effectiveness. Manufactured in WHO-GMP certified facilities, Optineuron supports nutritional supplementation, correction of vitamin deficiencies, and management of conditions requiring parenteral vitamin therapy.

Optineuron Vitamin Injection contains a balanced combination of water-soluble and fat-soluble vitamins, helping to maintain healthy metabolic function, support nervous system health, enhance immunity, and promote overall well-being. The injection is primarily indicated for patients with malnutrition, chronic illnesses, or vitamin deficiencies where oral supplementation is insufficient or not feasible.

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Optineuron Vitamin Injection is manufactured under strict GMP and quality standards, ensuring consistent potency, safety, and stability. The injection is supplied in sterile, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, clinics, nutritional therapy centers, and international pharmaceutical distributors.

FLUCONAZ-150 mg Tablets
Composition: Fluconazole 150 mg
International Trade Name: Diflucan®

FLUCONAZ-150 mg is a high-quality Fluconazole oral tablet, a trusted triazole antifungal agent equivalent to the internationally recognized Diflucan®. Manufactured in WHO-GMP certified facilities, FLUCONAZ-150 supports effective antifungal treatment programs across hospitals, clinics, and global healthcare settings.

Fluconazole works by inhibiting fungal cytochrome P450–dependent enzymes, disrupting ergosterol synthesis and compromising fungal cell membrane integrity. FLUCONAZ-150 mg Tablets are primarily indicated for the treatment of vaginal candidiasis, oropharyngeal and esophageal candidiasis, systemic candidal infections, cryptococcal meningitis, and other susceptible fungal infections.

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FLUCONAZ-150 mg Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, gynecology clinics, infectious disease centers, and international pharmaceutical distributors.

Glutimax 600 Injection
Composition: Glutathione 600mg Injection
International Trade Name: Glutathione®

Glutimax 600 is a high-quality Glutathione 600mg injection, a powerful antioxidant used to support detoxification, cellular protection, and skin health. Manufactured in WHO-GMP certified facilities, Glutimax Injection is supplied by trusted pharmaceutical exporters from India to support global healthcare and wellness programs.

Glutathione is a naturally occurring tripeptide that plays a critical role in neutralizing free radicals, reducing oxidative stress, and supporting liver and cellular detoxification processes. Glutimax 600 provides rapid systemic availability of glutathione, helping restore antioxidant balance and protect tissues from oxidative damage.

Glutimax 600 Injection is primarily indicated for the management of oxidative stress-related conditions, detoxification therapy, liver support, and as an adjunct in certain metabolic disorders. It is suitable for adult patients under medical supervision, particularly in hospital, clinical, or wellness therapy settings.

Glutimax 600 Glutathione Injection is manufactured under stringent GMP and pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, clinics, wellness centers, and international pharmaceutical distributors.

YAZ Tablets
Composition: Drospirenone 3 mg + Ethinylestradiol 0.02 mg
International Trade Name: YAZ®

YAZ is a high-quality combined oral contraceptive tablet, containing Drospirenone and Ethinylestradiol, equivalent to the internationally recognized YAZ®. Manufactured in WHO-GMP certified facilities, YAZ supports advanced women’s health and hormonal therapy programs worldwide.

Drospirenone is a progestin with anti-androgenic and anti-mineralocorticoid properties, while Ethinylestradiol is a synthetic estrogen that together provide effective contraception and hormonal balance. YAZ Tablets are primarily indicated for prevention of pregnancy, and also for management of moderate acne vulgaris and premenstrual dysphoric disorder (PMDD) in women choosing oral contraception.

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YAZ Tablets are manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for gynecology clinics, hospitals, family planning programs, and international pharmaceutical distributors.

Euthyrox 100 mcg Tablets
Composition: Levothyroxine Sodium 100 mcg
International Trade Name: Euthyrox®

Euthyrox 100 mcg is a high-quality Levothyroxine Sodium tablet, a trusted thyroid hormone replacement therapy equivalent to the internationally recognized Euthyrox®. Manufactured in WHO-GMP certified facilities, Euthyrox supports the management of hypothyroidism, goiter, and other thyroid hormone deficiency disorders.

Levothyroxine is a synthetic form of the naturally occurring thyroid hormone thyroxine (T4), which helps normalize thyroid hormone levels, regulate metabolism, and support overall growth and development. Euthyrox 100 mcg Tablets are primarily indicated for replacement therapy in hypothyroidism, suppression therapy in certain thyroid nodules or goiter, and adjunct therapy in thyroid cancer management.

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Euthyrox 100 mcg Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, endocrine care centers, and international pharmaceutical distributors.

Flonida 5% Cream
Composition: Fluorouracil 5% w/w
International Trade Name: Efudix®

Flonida 5% Cream is a high-quality topical chemotherapeutic preparation, a trusted therapy equivalent to the internationally recognized Efudix®. Manufactured in WHO-GMP certified facilities, Flonida supports advanced dermatologic oncology and pre-cancerous lesion management programs.

Fluorouracil is a pyrimidine analog antimetabolite that works by inhibiting DNA synthesis in rapidly dividing abnormal skin cells, effectively treating actinic keratosis, superficial basal cell carcinoma, and other precancerous skin lesions. Flonida 5% Cream is primarily indicated for treatment of actinic keratoses, superficial basal cell carcinoma, and other skin lesions responsive to topical 5-fluorouracil therapy.

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Flonida 5% Cream is manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The cream is supplied in secure, export-grade packaging with complete regulatory documentation, making it suitable for dermatology clinics, oncology centers, tertiary care hospitals, and international pharmaceutical distributors.

URSOLIEVA 300 mg Capsules
Composition: Ursodeoxycholic Acid 300 mg
International Trade Name: Ursofalk®

URSOLIEVA 300 mg is a high-quality Ursodeoxycholic Acid (UDCA) oral capsule, a trusted hepatobiliary therapy equivalent to the internationally recognized Ursofalk®. Manufactured in WHO-GMP certified facilities, URSOLIEVA supports advanced liver and biliary disorder management, particularly in patients with cholestatic liver diseases and cholesterol gallstones.

Ursodeoxycholic Acid is a naturally occurring hydrophilic bile acid that works by reducing cholesterol saturation of bile, improving bile flow, and protecting hepatocytes from bile acid–induced injury. URSOLIEVA 300 mg Capsules are primarily indicated for dissolution of cholesterol gallstones in selected patients, management of primary biliary cholangitis (PBC), and treatment of cholestatic liver disorders.

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URSOLIEVA 300 mg Capsules are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, hepatology clinics, gastroenterology centers, and international pharmaceutical distributors.

Morning Pills 1.5 mg Tablets
Composition: Levonorgestrel 1.5 mg
International Trade Name: Plan B®, Postinor®

Morning Pills 1.5 mg is a high-quality emergency contraceptive oral tablet, a trusted therapy equivalent to internationally recognized brands such as Plan B® and Postinor®. Manufactured in WHO-GMP certified facilities, Morning Pills supports advanced reproductive health programs by providing a safe and effective option for emergency contraception.

Levonorgestrel is a synthetic progestin that works by preventing ovulation, fertilization, or implantation of a fertilized egg, thereby reducing the risk of unintended pregnancy. Morning Pills 1.5 mg Tablets are primarily indicated for emergency contraception within 72 hours after unprotected intercourse or contraceptive failure.

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Morning Pills 1.5 mg Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, gynecology clinics, family planning centers, and international pharmaceutical distributors.

Walcobal Injection
Composition: Methylcobalamin 500 mcg / 1000 mcg per vial
International Trade Name: Methycobal®

Walcobal is a high-quality Methylcobalamin injection, a biologically active form of vitamin B12 widely used for the management of vitamin B12 deficiency, peripheral neuropathy, diabetic neuropathy, and neurological disorders. Manufactured in WHO-GMP certified facilities, Walcobal Injection is supplied by trusted pharmaceutical exporters from India to support advanced healthcare programs worldwide.

Methylcobalamin is an essential coenzyme form of vitamin B12 that plays a vital role in nerve regeneration, red blood cell formation, and DNA synthesis. Walcobal Injection is primarily indicated for treatment of neuropathies, vitamin B12 deficiency-related anemia, and as supportive therapy in neurological disorders.

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Walcobal Injection is manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, sterile, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, neurology clinics, diabetic care centers, and international pharmaceutical distributors.

Oseltaflux 75 mg Capsules
Composition: Oseltamivir Phosphate 75 mg
International Trade Name: Tamiflu®

Oseltaflux 75 mg is a high-quality Oseltamivir oral capsule, a trusted antiviral therapy equivalent to the internationally recognized Tamiflu®. Manufactured in WHO-GMP certified facilities, Oseltaflux supports advanced infectious disease management programs, particularly in the prevention and treatment of influenza A and B virus infections.

Oseltamivir is a neuraminidase inhibitor that works by blocking the action of viral neuraminidase, preventing the release and spread of influenza viruses in the body. Oseltaflux 75 mg Capsules are primarily indicated for treatment of uncomplicated influenza A and B in adults and children, and prophylaxis in individuals at high risk of influenza exposure.

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Oseltaflux 75 mg Capsules are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, infectious disease centers, and international pharmaceutical distributors.

Calcitas D3 Capsules
Composition: Vitamin D3 (Cholecalciferol)
International Trade Name: [Not Applicable / Custom Brand]

Calcitas D3 is a high-quality Vitamin D3 (Cholecalciferol) oral capsule, designed to support bone health, calcium absorption, and overall metabolic function. Manufactured in WHO-GMP certified facilities, Calcitas D3 is suitable for patients with vitamin D deficiency, osteoporosis, rickets, or other conditions requiring vitamin D supplementation.

Vitamin D3 is a fat-soluble vitamin that plays a key role in calcium and phosphorus metabolism, promoting healthy bone mineralization, muscle function, and immune support. Calcitas D3 Capsules are primarily indicated for prevention and treatment of vitamin D deficiency, maintenance of bone health, and support of overall metabolic balance.

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Calcitas D3 Capsules are manufactured under strict GMP and quality standards, ensuring consistent potency, safety, and stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, nutrition centers, and international pharmaceutical distributors.

SUNFORCE D3 Softgel Capsules
Composition: Cholecalciferol 60,000 IU per softgel
International Trade Name: SUNFORCE D3®

SUNFORCE D3 is a high-quality Cholecalciferol (Vitamin D3) softgel, widely used for the prevention and treatment of vitamin D deficiency. Manufactured in WHO-GMP certified facilities, SUNFORCE D3 supports advanced healthcare programs, particularly in maintaining bone health, calcium homeostasis, and overall musculoskeletal well-being.

Cholecalciferol is a fat-soluble vitamin (Vitamin D3) that is essential for calcium and phosphorus absorption, bone mineralization, and immune system regulation. SUNFORCE D3 Softgel Capsules are primarily indicated for vitamin D deficiency, rickets, osteomalacia, osteoporosis, and as a supportive supplement for musculoskeletal health.

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SUNFORCE D3 Softgel Capsules are manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, nutrition centers, wellness programs, and international pharmaceutical distributors.

Parkitidin Tablets
Composition: Amantadine Hydrochloride
International Trade Name: Symmetrel®

Parkitidin is a high-quality Amantadine oral tablet, a trusted therapy equivalent to the internationally recognized Symmetrel®. Manufactured in WHO-GMP certified facilities, Parkitidin supports advanced neurological treatment programs, particularly in the management of Parkinson’s disease and drug-induced extrapyramidal symptoms.

Amantadine is a dopaminergic agent and NMDA receptor antagonist that works by enhancing dopamine release and inhibiting its reuptake, thereby improving motor function and reducing symptoms such as rigidity, tremor, and bradykinesia. Parkitidin Tablets are primarily indicated for symptomatic treatment of Parkinson’s disease, management of drug-induced extrapyramidal reactions, and as adjunct therapy in certain movement disorders.

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Parkitidin Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, neurology clinics, tertiary care centers, and international pharmaceutical distributors.

Ensorex 50 mg Tablets
Composition: Amantadine Hydrochloride 50 mg
International Trade Name: Symmetrel®

Ensorex 50 mg is a high-quality Amantadine oral tablet, a trusted antiviral and antiparkinsonian therapy equivalent to the internationally recognized Symmetrel®. Manufactured in WHO-GMP certified facilities, Ensorex supports advanced neurological and antiviral treatment programs, particularly in Parkinson’s disease and influenza A infections.

Amantadine works by enhancing dopaminergic activity in the central nervous system and exhibiting antiviral effects against influenza A virus, providing symptomatic relief and functional improvement. Ensorex 50 mg Tablets are primarily indicated for management of Parkinson’s disease and drug-induced extrapyramidal reactions, and prophylaxis or treatment of influenza A virus infections.

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Ensorex 50 mg Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, neurology clinics, tertiary care centers, and international pharmaceutical distributors.

GLOBUCEL 5 g Injection
Composition: Human Normal Immunoglobulin IP 5% Solution (5 g)
Dosage Form: Solution for Intravenous (IV) Use
International Trade Name: GLOBUCEL

GLOBUCEL 5 g Injection is a premium-quality Human Normal Immunoglobulin (HNI) IP 5% Solution, formulated for intravenous administration to support immune replacement and immunomodulatory therapy. Manufactured in WHO-GMP compliant, plasma fractionation facilities, GLOBUCEL is supplied by reliable pharmaceutical manufacturers and exporters from India, meeting global standards for plasma-derived biologics.

Human Normal Immunoglobulin is a highly purified preparation of polyvalent IgG antibodies, obtained from rigorously screened human plasma donors. It functions by providing passive immunity, neutralizing infectious agents, and regulating abnormal immune responses, thereby enhancing immune defense and restoring immune balance in vulnerable patients.

GLOBUCEL 5 g Injection undergoes multiple viral inactivation and removal steps, ensuring maximum safety, purity, and consistent clinical efficacy in compliance with Indian Pharmacopoeia (IP) and international biologics quality norms.

GLOBUCEL 5 g Human Normal Immunoglobulin Injection is primarily indicated for the treatment of primary and secondary immunodeficiency disorders, immune thrombocytopenic purpura (ITP), Guillain-Barré syndrome, chronic inflammatory demyelinating polyneuropathy (CIDP), Kawasaki disease, and other autoimmune, neurological, and hematological conditions, as prescribed by healthcare professionals.

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GLOBUCEL 5 g Injection is produced under stringent GMP, biologics safety, and cold-chain controlled conditions, ensuring long-term stability, safety, and therapeutic reliability. The product is supplied in secure, tamper-evident, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for tertiary care hospitals, ICUs, neurology and hematology centers, government immunotherapy programs, and international pharmaceutical distributors.

BOSENZER-125 Tablets
Composition: Bosentan 125 mg
International Trade Name: Tracleer®

BOSENZER-125 is a high-quality Bosentan oral tablet, a trusted endothelin receptor antagonist equivalent to the internationally recognized Tracleer®. Manufactured in WHO-GMP certified facilities, BOSENZER-125 supports advanced pulmonary arterial hypertension (PAH) management programs, helping to improve exercise capacity and slow disease progression.

Bosentan works by blocking endothelin-1 receptors (ET-A and ET-B), which reduces vasoconstriction and vascular remodeling in pulmonary arteries, thereby lowering pulmonary arterial pressure. BOSENZER-125 Tablets are primarily indicated for treatment of pulmonary arterial hypertension (PAH) in adult patients, including idiopathic or heritable PAH and PAH associated with connective tissue disease.

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BOSENZER-125 Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for cardiology centers, tertiary care hospitals, PAH clinics, and international pharmaceutical distributors.

Apigat 2.5 mg Tablets
Composition: Apixaban 2.5 mg
International Trade Name: Eliquis®

Apigat 2.5 mg is a high-quality Apixaban tablet, a trusted oral anticoagulant equivalent to the internationally recognized Eliquis®. Manufactured in WHO-GMP certified facilities, Apigat supports advanced clinical programs for the prevention and treatment of thromboembolic disorders.

Apixaban is a direct oral anticoagulant (DOAC) that selectively inhibits Factor Xa, preventing thrombin generation and thrombus formation. Apigat 2.5 mg Tablets are primarily indicated for prevention of stroke and systemic embolism in non-valvular atrial fibrillation, treatment and prevention of deep vein thrombosis (DVT) and pulmonary embolism (PE), and prophylaxis after orthopedic surgery.

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Apigat 2.5 mg Tablets are manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, cardiology clinics, thromboembolism treatment centers, and international pharmaceutical distributors.

Folisurge 900 IU Injection
Composition: Recombinant Follicle Stimulating Hormone (rFSH) 900 IU
International Trade Name: Bravelle®

Folisurge 900 IU is a high-quality recombinant FSH injection, a trusted fertility treatment equivalent to the internationally recognized Bravelle®. Manufactured in WHO-GMP certified facilities, Folisurge supports advanced assisted reproductive technology (ART) programs, helping patients undergoing ovulation induction or controlled ovarian stimulation.

Recombinant Follicle Stimulating Hormone (rFSH) is a bioengineered glycoprotein hormone that stimulates the development of ovarian follicles, facilitating ovulation and improving the chances of conception. Folisurge 900 IU Injection is primarily indicated for women undergoing fertility treatments, including in vitro fertilization (IVF), intrauterine insemination (IUI), or other ART procedures.

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Folisurge 900 IU Injection is manufactured under stringent GMP and biologics quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for fertility clinics, IVF centers, tertiary care hospitals, and international pharmaceutical distributors.

Folisurge 1200 IU Injection
Composition: Recombinant Follicle Stimulating Hormone (Follitropin Alfa) 1200 IU
International Trade Name: Gonal-F®

Folisurge 1200 is a high-quality Recombinant Follicle Stimulating Hormone (FSH) injection, a trusted fertility treatment equivalent to the internationally recognized Gonal-F®. Manufactured in WHO-GMP certified facilities, Folisurge supports advanced reproductive healthcare programs, particularly in assisted reproductive technology (ART), controlled ovarian stimulation (COS), and infertility management.

Follitropin alfa is a recombinant form of human FSH that stimulates follicular development and maturation in women undergoing fertility treatment. Folisurge 1200 IU Injection is primarily indicated for ovarian stimulation in anovulatory women, controlled ovarian hyperstimulation prior to ART procedures like IVF, and in men with hypogonadotropic hypogonadism to induce spermatogenesis.

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Folisurge 1200 IU Injection is manufactured under strict GMP and biologics-quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for fertility clinics, assisted reproduction centers, tertiary care hospitals, and international pharmaceutical distributors.

Grifols Albumin 20% Injection
Composition: Human Albumin Solution 20% w/v
International Trade Name: Human Albumin (Grifols)

Grifols Albumin 20% is a high-quality human albumin solution derived from screened human plasma, manufactured using advanced fractionation and purification technologies by Grifols, a globally recognized leader in plasma-derived therapies. Produced in EU- and WHO-GMP certified facilities, Grifols Albumin 20% is supplied to support critical care, hepatology, nephrology, and emergency medicine programs worldwide.

Human Albumin 20% is a concentrated plasma protein solution used to restore and maintain intravascular volume and oncotic pressure in patients with hypoalbuminemia or fluid imbalance. Grifols Albumin 20% Injection is primarily indicated for conditions such as liver cirrhosis with ascites, nephrotic syndrome, burns, shock, major surgery, trauma, and therapeutic plasma exchange, where colloid volume expansion is clinically required.

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Grifols Albumin 20% is manufactured under stringent GMP, viral inactivation, and biologics safety standards, ensuring high purity, optimal osmotic activity, and excellent tolerability. The product is supplied in sterile, ready-to-use infusion bottles with cold-chain compliant, export-grade packaging and complete regulatory documentation, making it suitable for intensive care units (ICUs), tertiary care hospitals, transplant centers, government health programs, and international pharmaceutical distributors.

Immuglo 5% / 10% Human Normal Immunoglobulin Injection
Composition: Human Normal Immunoglobulin (IVIG) 5% / 10%
International Trade Name: Sandoglobulin®

Immuglo is a high-quality Human Normal Immunoglobulin (IVIG) injection, a trusted immunotherapy equivalent to the internationally recognized Sandoglobulin®. Manufactured in WHO-GMP certified facilities, Immuglo supports advanced immunodeficiency management, autoimmune therapy, and prophylactic treatment against infections in patients with compromised or weakened immune systems.

Human normal immunoglobulin contains pooled antibodies from healthy donors, providing passive immunity and enhancing the body’s defense against a wide range of infections. Immuglo IVIG Injection is primarily indicated for primary and secondary immunodeficiency disorders, immune thrombocytopenic purpura (ITP), chronic inflammatory demyelinating polyneuropathy (CIDP), Kawasaki disease, and other immune-mediated conditions.

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Immuglo Human Normal Immunoglobulin is manufactured under stringent GMP and biologics-quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in sterile, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, tertiary care centers, immunology clinics, and international pharmaceutical distributors.

Arsenam 10 mg Injection
Composition: Arsenic Trioxide 10 mg
International Trade Name: Trisenox®

Arsenam 10 mg is a high-quality Arsenic Trioxide injection, a trusted chemotherapeutic agent equivalent to the internationally recognized Trisenox®. Manufactured in WHO-GMP certified facilities, Arsenam supports advanced oncology treatment programs, particularly in the management of acute promyelocytic leukemia (APL) and other specific hematologic malignancies.

Arsenic trioxide works by inducing apoptosis and promoting differentiation of malignant cells, providing targeted cytotoxic effects against leukemic cells. Arsenam 10 mg Injection is primarily indicated for treatment of newly diagnosed or relapsed/refractory acute promyelocytic leukemia in patients not suitable for intensive chemotherapy, either as monotherapy or in combination regimens.

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Arsenam 10 mg Injection is manufactured under strict GMP and biologics-quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in sterile, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for oncology centers, tertiary care hospitals, hematology clinics, and international pharmaceutical distributors.

Plasbumin 20
Composition: Human Albumin 20% Solution
International Trade Name: Grifols Albumin®

Plasbumin 20 is a high-quality Human Albumin 20% solution, a plasma-derived protein used for restoring and maintaining blood volume, plasma protein levels, and oncotic pressure in various clinical conditions. Manufactured in WHO-GMP certified facilities, Plasbumin 20 is supplied by trusted pharmaceutical exporters from India to support global critical care, surgical, and therapeutic programs.

Human albumin is a natural plasma protein that helps maintain colloid osmotic pressure, supports circulatory stability, and facilitates transport of various endogenous and exogenous substances. Plasbumin 20 provides rapid plasma expansion and restores albumin levels in patients with hypovolemia, hypoalbuminemia, burns, liver disease, and other conditions requiring plasma protein supplementation.

Plasbumin 20 is primarily indicated for volume replacement in hypovolemia, hypoalbuminemia, burns, shock, and during surgical or critical care management. It is suitable for adult and pediatric patients under medical supervision, particularly in intensive care and hospital settings.

Plasbumin 20 Human Albumin 20% is manufactured under stringent GMP and plasma quality standards, ensuring consistent efficacy, safety, and viral inactivation. The solution is supplied in secure, tamper-proof, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, blood banks, critical care units, and international pharmaceutical distributors.

Azicip 500 Tablets
Composition: Azithromycin 500 mg
International Trade Name: Zithromax®

Azicip 500 is a high-quality Azithromycin oral tablet, a trusted macrolide antibiotic equivalent to the internationally recognized Zithromax®. Manufactured in WHO-GMP certified facilities, Azicip 500 supports advanced antibacterial treatment programs, particularly in the management of respiratory, skin, soft tissue, and sexually transmitted infections.

Azithromycin is a broad-spectrum macrolide antibiotic that works by inhibiting bacterial protein synthesis, providing effective activity against a wide range of Gram-positive and Gram-negative pathogens. Azicip 500 Tablets are primarily indicated for treatment of upper and lower respiratory tract infections, skin and soft tissue infections, otitis media, pharyngitis/tonsillitis, and certain sexually transmitted infections such as chlamydia.

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Azicip 500 Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, tertiary care centers, pharmacies, and international pharmaceutical distributors.

Biomycin-500 Tablets
Composition: Clarithromycin 500 mg
International Trade Name: Biaxin®

Biomycin-500 is a high-quality Clarithromycin oral tablet, a trusted macrolide antibiotic equivalent to the internationally recognized Biaxin®. Manufactured in WHO-GMP certified facilities, Biomycin-500 supports advanced antibacterial therapy programs, particularly in the treatment of respiratory tract infections, skin infections, and Helicobacter pylori-associated peptic ulcers.

Clarithromycin is a broad-spectrum macrolide antibiotic that works by inhibiting bacterial protein synthesis, effectively combating susceptible Gram-positive and Gram-negative bacteria. Biomycin-500 Tablets are primarily indicated for treatment of community-acquired pneumonia, chronic bronchitis exacerbations, sinusitis, pharyngitis/tonsillitis, skin and soft tissue infections, and H. pylori eradication as part of combination therapy.

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Biomycin-500 Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, tertiary care centers, and international pharmaceutical distributors.

Phoscut 400 mg Tablets
Composition: Sevelamer Carbonate 400 mg
International Trade Name: Renvela®

Phoscut 400 mg is a high-quality Sevelamer Carbonate tablet, a trusted phosphate binder equivalent to the internationally recognized Renvela®. Manufactured in WHO-GMP certified facilities, Phoscut supports the management of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis, helping to maintain normal phosphate levels and reduce associated complications.

Sevelamer carbonate is a non-calcium, non-metal phosphate binder that binds dietary phosphate in the gastrointestinal tract, preventing its absorption and thereby helping to control serum phosphate levels without increasing calcium load. Phoscut 400 mg is primarily indicated for the management of hyperphosphatemia in adult and pediatric CKD patients on hemodialysis or peritoneal dialysis.

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Phoscut 400 mg is manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for dialysis centers, nephrology clinics, tertiary care hospitals, and international pharmaceutical distributors.

GESTLIEVA 400 mg Capsules
Composition: Progesterone 400 mg
International Trade Name: Utrogestan®

GESTLIEVA 400 mg is a high-quality micronized Progesterone oral/vaginal capsule, a trusted hormonal therapy equivalent to the internationally recognized Utrogestan®. Manufactured in WHO-GMP certified facilities, GESTLIEVA supports advanced women’s health, fertility, and hormonal replacement therapy programs worldwide.

Progesterone is a naturally occurring female sex hormone essential for regulating the menstrual cycle, supporting implantation, and maintaining pregnancy. GESTLIEVA 400 mg Capsules are primarily indicated for luteal phase support in assisted reproductive technology (ART), prevention of threatened or recurrent miscarriage, management of progesterone deficiency, and hormone replacement therapy (HRT).

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GESTLIEVA 400 mg Capsules are manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for fertility clinics, gynecology hospitals, IVF centers, and international pharmaceutical distributors.

Paxobrook Tablets
Composition: Nirmatrelvir + Ritonavir
International Trade Name: Paxlovid®

Paxobrook is a high-quality antiviral oral tablet combination, a trusted therapy equivalent to the internationally recognized Paxlovid®. Manufactured in WHO-GMP certified facilities, Paxobrook supports advanced COVID-19 treatment programs, particularly in high-risk adult patients with mild to moderate SARS-CoV-2 infection.

Nirmatrelvir is a protease inhibitor that prevents viral replication, while Ritonavir boosts Nirmatrelvir’s plasma concentration by inhibiting CYP3A-mediated metabolism, enhancing antiviral efficacy. Paxobrook Tablets are primarily indicated for treatment of mild to moderate COVID-19 in adults and pediatric patients (12 years and older weighing ≥40 kg) who are at high risk of progressing to severe disease, including hospitalization or death.

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Paxobrook Tablets are manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, COVID-19 care centers, tertiary care facilities, and international pharmaceutical distributors.

Phoscut 800 mg Tablets
Composition: Sevelamer Carbonate 800 mg
International Trade Name: Renvela®

Phoscut 800 mg is a high-quality Sevelamer Carbonate oral tablet, a trusted phosphate binder equivalent to the internationally recognized Renvela®. Manufactured in WHO-GMP certified facilities, Phoscut supports advanced chronic kidney disease (CKD) management programs, particularly in patients undergoing dialysis with hyperphosphatemia.

Sevelamer carbonate is a non-calcium, non-metal phosphate binder that works by binding dietary phosphate in the gastrointestinal tract, reducing its absorption, and helping maintain normal serum phosphate levels without increasing calcium load. Phoscut 800 mg Tablets are primarily indicated for management of hyperphosphatemia in adult and pediatric CKD patients on hemodialysis or peritoneal dialysis.

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Phoscut 800 mg Tablets are manufactured under strict GMP and biologics-quality standards, ensuring consistent efficacy, safety, and long-term stability. The tablets are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for dialysis centers, nephrology clinics, tertiary care hospitals, and international pharmaceutical distributors.

Gamma Safe 5% – Human Normal Immunoglobulin
Composition: Human Normal Immunoglobulin IP 5% (5 g/vial)
International Trade Name: Gamma Safe

Gamma Safe 5% is a high-quality, sterile Human Normal Immunoglobulin (HNIG) formulation, manufactured in WHO-GMP certified facilities and supplied by trusted pharmaceutical exporters from India to support global immunotherapy and clinical immunology programs.

Human Normal Immunoglobulin (Gamma Globulin) is a purified preparation of polyvalent IgG antibodies derived from healthy human plasma. Gamma Safe 5% provides passive immunity by supplying a broad spectrum of antibodies, enhancing the body’s defense against infections and immune deficiencies. It is primarily indicated for the treatment of primary and secondary immunodeficiency disorders, prophylaxis in immunocompromised patients, post-exposure prophylaxis for certain infections, and supportive therapy in various autoimmune and hematological conditions under medical supervision.

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Gamma Safe Human Normal Immunoglobulin IP 5% 5 g is manufactured under stringent GMP and biologics quality standards, ensuring consistent efficacy, safety, viral inactivation, and stability. The injection is supplied in secure, sterile, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, tertiary care centers, immunology clinics, government health programs, and international pharmaceutical distributors.

Bontol Infusion
Composition: Mannitol and Glycerin for Injection
International Trade Name: Osmitrol®

Bontol is a high-quality osmotic diuretic infusion, a trusted therapy equivalent to the internationally recognized Osmitrol®. Manufactured in WHO-GMP certified facilities, Bontol supports advanced critical care and neurology programs, particularly in the management of elevated intracranial pressure (ICP) and cerebral edema.

Mannitol and Glycerin work as osmotic agents that draw water out of tissues and reduce cerebral swelling, thereby decreasing intracranial pressure and improving cerebral perfusion. Bontol Infusion is primarily indicated for reduction of raised intracranial pressure in head trauma, stroke, brain tumors, and postoperative cerebral edema, as well as promotion of renal excretion in certain cases.

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Bontol Infusion is manufactured under strict GMP and quality standards, ensuring consistent efficacy, safety, and stability. The infusion is supplied in sterile, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, neurology and ICU centers, tertiary care hospitals, and international pharmaceutical distributors.

HYDROXYRA 250 Capsules
Composition: Hydroxyurea 250 mg
International Trade Names: Hydrea®, Litalir®, Droxia®, Siklos®

HYDROXYRA 250 is a high-quality Hydroxyurea capsule, a trusted oral chemotherapeutic and hematologic agent equivalent to internationally recognized brands like Hydrea®, Litalir®, Droxia®, and Siklos®. Manufactured in WHO-GMP certified facilities, HYDROXYRA supports advanced clinical programs for the management of myeloproliferative disorders, sickle cell anemia, and certain types of cancers.

Hydroxyurea is a ribonculeotide reductase inhibitor that works by inhibiting DNA synthesis, leading to reduced proliferation of abnormal blood cells. HYDROXYRA 250 Capsules are primarily indicated for sickle cell disease to reduce vaso-occlusive crises, chronic myeloid leukemia (CML), polycythemia vera, and other myeloproliferative disorders.

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HYDROXYRA 250 Capsules are manufactured under stringent GMP and quality standards, ensuring consistent efficacy, safety, and long-term stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, hematology clinics, oncology centers, government healthcare programs, and international pharmaceutical distributors.

PEMETYRA 500 mg Injection
Composition: Pemetrexed Disodium 500 mg per vial
International Trade Name: Alimta®

PEMETYRA 500 mg is a high-quality Pemetrexed injection, a trusted antifolate chemotherapeutic agent equivalent to the internationally recognized Alimta®. Manufactured in WHO-GMP certified facilities, PEMETYRA supports advanced oncology treatment programs worldwide, particularly in malignant pleural mesothelioma and non-small cell lung cancer (NSCLC).

Pemetrexed is a multitargeted antifolate cytotoxic agent that inhibits several key enzymes involved in nucleotide synthesis, preventing cancer cell replication and growth. PEMETYRA 500 mg Injection is primarily indicated for first-line and maintenance treatment of non-squamous NSCLC and for treatment of unresectable malignant pleural mesothelioma, often in combination with cisplatin or as monotherapy.

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PEMETYRA 500 mg Injection is manufactured under stringent GMP and biologics quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, sterile, cold-chain compliant packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, cancer treatment programs, and international pharmaceutical distributors.

L Aspyra 10,000 IU Injection
Composition: Asparaginase 10,000 IU
International Trade Name: Elspar®

L Aspyra 10,000 IU is a high-quality Asparaginase injection, a trusted chemotherapeutic enzyme therapy equivalent to the internationally recognized Elspar®. Manufactured in WHO-GMP certified facilities, L Aspyra supports advanced oncology treatment programs, particularly in the management of acute lymphoblastic leukemia (ALL).

Asparaginase is an enzyme that depletes circulating L-asparagine, an amino acid essential for the growth of leukemia cells, thereby inhibiting cancer cell proliferation. L Aspyra 10,000 IU Injection is primarily indicated for induction and consolidation therapy in pediatric and adult patients with acute lymphoblastic leukemia, either as monotherapy or in combination chemotherapy protocols.

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L Aspyra 10,000 IU Injection is manufactured under stringent GMP and biologics-quality standards, ensuring consistent efficacy, safety, and stability. The injection is supplied in sterile, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for oncology centers, tertiary care hospitals, hematology clinics, and international pharmaceutical distributors.

EXTEND Omega-3 Fatty Acid, Vitamins & Minerals Capsules
Composition: Omega-3 Fatty Acids (EPA & DHA) with Essential Vitamins and Minerals
International Trade Name: [Not Applicable / Nutraceutical Brand]

EXTEND Omega-3 Capsules are a high-quality nutraceutical formulation designed to support cardiovascular health, brain function, immunity, and overall metabolic balance. Manufactured in WHO-GMP certified facilities, EXTEND supports daily nutritional supplementation programs for individuals with increased dietary requirements or nutritional deficiencies.

Omega-3 fatty acids, including EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid), play a vital role in maintaining heart health, supporting cognitive function, reducing inflammation, and promoting joint mobility. The added vitamins and minerals help support energy metabolism, immune defense, bone strength, and overall well-being. EXTEND Capsules are primarily indicated for nutritional supplementation, cardiovascular support, cognitive health, and general wellness maintenance.

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EXTEND Omega-3 Fatty Acid, Vitamins & Minerals Capsules are manufactured under strict GMP and quality standards, ensuring consistent potency, safety, and stability. The capsules are supplied in secure, export-grade packaging with complete regulatory documentation, making them suitable for hospitals, clinics, wellness centers, pharmacies, and international nutraceutical distributors.