Unnati Pharmax

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

ARTECAN 120 mg Injection
Composition: Artesunate 120 mg
International Trade Name: [Not Applicable / Custom Brand]

ARTECAN 120 mg is a high-quality Artesunate injection, a trusted antimalarial therapy used for the treatment of severe and complicated malaria, particularly infections caused by Plasmodium falciparum. Manufactured in WHO-GMP certified facilities, ARTECAN supports advanced malaria treatment programs in hospitals, clinics, and endemic regions.

Artesunate is a semi-synthetic derivative of artemisinin that works by rapidly reducing parasitemia through potent antiplasmodial activity, leading to effective and fast relief in severe malaria cases. ARTECAN 120 mg Injection is primarily indicated for treatment of severe malaria in adults and children, especially in Plasmodium falciparum infections, and as part of combination therapy for resistant cases.

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ARTECAN 120 mg Injection is manufactured under strict GMP and 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 hospitals, tertiary care centers, tropical disease clinics, 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.

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.

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.

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.

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.

Tiova Inhaler
Composition: Tiotropium Bromide Inhalation Powder 18 mcg per actuation
International Trade Name: Tiotropium

Tiova Inhaler is a high-quality long-acting bronchodilator containing tiotropium bromide, a muscarinic (anticholinergic) receptor antagonist, formulated for convenient inhalation therapy. Manufactured in WHO-GMP certified facilities, Tiova Inhaler is supplied by trusted pharmaceutical exporters from India to support global respiratory care programs, particularly for patients with chronic obstructive pulmonary disease (COPD) and chronic bronchitis.

Tiotropium bromide works by selectively inhibiting M3 receptors in the airway smooth muscle, producing prolonged bronchodilation, improving airflow, and reducing symptoms of breathlessness. Tiova Inhaler is primarily indicated for the maintenance treatment of airflow obstruction in patients with COPD, including chronic bronchitis and emphysema. It helps improve lung function, exercise tolerance, and quality of life when used as part of long-term therapy.

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Tiova Inhaler is manufactured under stringent GMP and inhalation device quality standards, ensuring accurate dosing, safety, and consistent efficacy. The inhaler is supplied in compact, patient-friendly, and export-grade packaging with complete regulatory documentation, making it suitable for hospitals, pulmonary clinics, respiratory therapy programs, and international pharmaceutical distributors.

Vitamin D3 Injection – Cal D 3
Composition: Cholecalciferol (Vitamin D3) Injection
International Trade Name: Vitamin D3 (Cholecalciferol) Injection

Cal D 3 is a high-quality Vitamin D3 (Cholecalciferol) Injection formulated for rapid correction and management of Vitamin D deficiency. Manufactured in WHO-GMP certified facilities, Cal D 3 Injection is supplied by trusted pharmaceutical exporters from India to support global nutritional and metabolic health programs, particularly in conditions requiring parenteral Vitamin D supplementation.

Vitamin D3 (Cholecalciferol) plays a crucial role in calcium and phosphorus metabolism, bone mineralization, and musculoskeletal health. Cal D 3 Injection is primarily indicated for the treatment and prevention of Vitamin D deficiency, osteoporosis, osteomalacia, rickets, hypocalcemia, and related metabolic bone disorders, especially in patients with malabsorption syndromes or where oral therapy is ineffective or contraindicated.

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Cal D 3 Vitamin D3 Injection is manufactured under stringent GMP and pharmaceutical quality standards, ensuring consistent potency, sterility, stability, and patient safety. The injection is supplied in secure, light-protected, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, clinics, orthopedic and endocrinology centers, government health programs, and international pharmaceutical distributors.

Budetrol 200 Inhalation
Composition: Budesonide 200 mcg + Formoterol Fumarate 6 mcg Inhalation
International Trade Name: Budesonide + Formoterol Inhaler (ICS/LABA Combination)

Budetrol 200 is a high-quality combination inhalation therapy containing Budesonide and Formoterol Fumarate, designed for effective long-term management of chronic respiratory disorders. Manufactured in WHO-GMP certified facilities, Budetrol 200 Inhalation is supplied by trusted pharmaceutical exporters from India to support global respiratory care programs, particularly in asthma and chronic obstructive pulmonary disease (COPD).

Budesonide is an inhaled corticosteroid (ICS) that reduces airway inflammation, while Formoterol Fumarate is a long-acting beta-2 agonist (LABA) that provides sustained bronchodilation. Together, this synergistic combination delivers rapid symptom relief along with long-term control of airway inflammation. Budetrol 200 Inhalation is primarily indicated for the maintenance treatment of bronchial asthma and COPD in patients requiring combined corticosteroid and long-acting bronchodilator therapy.

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Budetrol 200 Formoterol Fumarate and Budesonide Inhalation is manufactured under stringent GMP and pharmaceutical quality standards, ensuring consistent dose delivery, optimal particle size distribution, safety, and therapeutic efficacy. The inhaler is supplied in secure, moisture-protected, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, pulmonology clinics, government respiratory health programs, retail pharmacies, 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.

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.

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.

Tiova Synchrobreathe Inhaler
Composition: Tiotropium Bromide Inhalation
International Trade Name: Spiriva®

Tiova Synchrobreathe is a high-quality Tiotropium Bromide dry powder inhaler, a trusted long-acting anticholinergic bronchodilator equivalent to the internationally recognized Spiriva®. Manufactured in WHO-GMP certified facilities, Tiova Synchrobreathe supports advanced respiratory disease management programs, particularly for patients with chronic obstructive pulmonary disease (COPD) and asthma.

Tiotropium Bromide is a long-acting muscarinic antagonist (LAMA) that works by relaxing bronchial smooth muscles and maintaining airway dilation, thereby improving airflow and reducing exacerbations. Tiova Synchrobreathe is primarily indicated for maintenance treatment of COPD, including chronic bronchitis and emphysema, and as add-on maintenance therapy in asthma.

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Tiova Synchrobreathe is manufactured under stringent GMP and device-quality standards, ensuring consistent dose delivery, safety, and long-term performance. The inhaler is supplied in secure, patient-friendly, export-grade packaging with complete regulatory documentation, making it suitable for pulmonology clinics, hospitals, respiratory care centers, and international pharmaceutical distributors.

Asthalin Inhaler
Composition: Salbutamol Inhalation IP 100 mcg per actuation
International Trade Name: Ventolin®

Asthalin is a high-quality Salbutamol metered-dose inhaler (MDI), a trusted short-acting β2-agonist (SABA) equivalent to the internationally recognized Ventolin®. Manufactured in WHO-GMP certified facilities, Asthalin supports effective respiratory care and emergency bronchodilation, particularly in patients with asthma and chronic obstructive pulmonary disease (COPD).

Salbutamol works by selectively stimulating β2-adrenergic receptors in bronchial smooth muscle, leading to rapid bronchodilation and relief from bronchospasm. Asthalin Inhaler 100 mcg is primarily indicated for relief and prevention of bronchospasm in asthma, COPD, exercise-induced bronchoconstriction, and other reversible obstructive airway diseases.

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Asthalin Inhaler is manufactured under strict GMP and quality standards, ensuring consistent dose delivery, safety, and performance. The inhaler is supplied in secure, tamper-evident, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, pulmonology clinics, emergency care units, pharmacies, and international pharmaceutical distributors.

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.

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.

Amoxyheal CV 1000 mg Tablets
Composition: Amoxicillin 875 mg + Potassium Clavulanate 125 mg
International Trade Name: Augmentin®

Amoxyheal CV 1000 mg is a high-quality combination antibiotic tablet, a trusted therapy equivalent to the internationally recognized Augmentin®. Manufactured in WHO-GMP certified facilities, Amoxyheal CV supports advanced antibacterial treatment programs, particularly in the management of respiratory tract infections, skin infections, urinary tract infections, and other bacterial infections.

Amoxicillin is a broad-spectrum β-lactam antibiotic that inhibits bacterial cell wall synthesis, while Potassium Clavulanate is a β-lactamase inhibitor that protects Amoxicillin from degradation by resistant bacteria. Amoxyheal CV 1000 mg Tablets are primarily indicated for treatment of moderate to severe infections caused by susceptible bacteria, including sinusitis, otitis media, lower respiratory tract infections, skin and soft tissue infections, and urinary tract infections.

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Amoxyheal CV 1000 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, clinics, tertiary care centers, 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.

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.

PTH-30 Tablets
Composition: Cinacalcet 30 mg
International Trade Name: Mimpara® / Sensipar®

PTH-30 is a high-quality Cinacalcet tablet, a trusted oral calcimimetic agent equivalent to internationally recognized brands like Mimpara® and Sensipar®. Manufactured in WHO-GMP certified facilities, PTH-30 supports advanced clinical programs for the management of secondary hyperparathyroidism in chronic kidney disease (CKD) patients on dialysis and hypercalcemia associated with parathyroid carcinoma.

Cinacalcet is a calcimimetic agent that works by increasing the sensitivity of calcium-sensing receptors on parathyroid cells, thereby reducing parathyroid hormone (PTH) secretion and helping maintain balanced calcium and phosphate levels. PTH-30 Tablets are primarily indicated for secondary hyperparathyroidism in CKD patients, parathyroid carcinoma, and related calcium metabolism disorders.

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PTH-30 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, nephrology clinics, dialysis centers, endocrine 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.

Hytrin 2 mg Tablets
Composition: Terazosin Hydrochloride 2 mg
International Trade Name: Hytrin®

Hytrin 2 mg is a high-quality Terazosin oral tablet, a trusted alpha-1 adrenergic receptor antagonist equivalent to the internationally recognized Hytrin®. Manufactured in WHO-GMP certified facilities, Hytrin supports advanced management of benign prostatic hyperplasia (BPH) and hypertension, improving patient quality of life.

Terazosin works by relaxing smooth muscles in the prostate and bladder neck, improving urinary flow in men with BPH, and reducing vascular resistance, thereby helping control blood pressure. Hytrin 2 mg Tablets are primarily indicated for treatment of symptoms of benign prostatic hyperplasia and management of mild to moderate essential hypertension.

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Hytrin 2 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, urology clinics, tertiary care centers, and international pharmaceutical distributors.

Ceftrox 1g / 2g Injection
Composition: Ceftriaxone Sodium Injection 1g / 2g
International Trade Name: Rocephin®

Ceftrox is a high-quality Ceftriaxone Injection, a trusted broad-spectrum third-generation cephalosporin antibiotic, equivalent to the internationally recognized Rocephin®. Manufactured in WHO-GMP certified facilities, Ceftrox Injection is supplied by reliable pharmaceutical exporters from India to support advanced global healthcare programs, particularly in the treatment of serious bacterial infections.

Ceftriaxone is a potent β-lactam antibiotic that works by inhibiting bacterial cell wall synthesis, providing effective treatment against a wide range of Gram-positive and Gram-negative pathogens. Ceftrox Injection is primarily indicated for severe infections, including septicemia, respiratory tract infections, urinary tract infections, meningitis, gonorrhea, and surgical prophylaxis.

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Ceftrox Injection is manufactured under strict GMP and 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 hospital infusion centers, tertiary care hospitals, government healthcare programs, 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.

Ciscure 0.25 mg / 3 mg Injection
Composition: Cetrorelix Acetate Injection
International Trade Name: Cetrotide®

Ciscure is a high-quality Cetrorelix Acetate injection, a trusted gonadotropin-releasing hormone (GnRH) antagonist equivalent to the internationally recognized Cetrotide®. Manufactured in WHO-GMP certified facilities, Ciscure supports advanced fertility treatment programs, particularly in assisted reproductive technology (ART) and controlled ovarian stimulation (COS) protocols.

Cetrorelix acetate works by suppressing premature luteinizing hormone (LH) surges, allowing precise control of ovulation during fertility treatments. Ciscure Injection is primarily indicated for prevention of premature ovulation in women undergoing controlled ovarian stimulation for in vitro fertilization (IVF) procedures.

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Ciscure Injection is manufactured under stringent GMP and biologics-quality standards, ensuring consistent efficacy, safety, and 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.

Eurelix Injection
Composition: Cetrorelix Acetate Injection
International Trade Name: Cetrotide®

Eurelix is a high-quality Cetrorelix Acetate injection, a trusted gonadotropin-releasing hormone (GnRH) antagonist equivalent to the internationally recognized Cetrotide®. Manufactured in WHO-GMP certified facilities, Eurelix is supplied by reliable pharmaceutical exporters from India to support advanced fertility and assisted reproductive technology (ART) programs worldwide.

Cetrorelix acetate acts by rapidly and competitively inhibiting GnRH receptors, thereby preventing premature luteinizing hormone (LH) surges during controlled ovarian stimulation. Eurelix Injection is primarily indicated for the prevention of premature ovulation in women undergoing controlled ovarian stimulation as part of in vitro fertilization (IVF) and other ART procedures.

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Eurelix 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, export-grade packaging with complete regulatory documentation, making it suitable for fertility clinics, assisted reproduction centers, tertiary care hospitals, and international pharmaceutical distributors.

Beeta-L Injection
Composition: Labetalol Hydrochloride Injection
International Trade Name: Trandate®

Beeta-L is a high-quality Labetalol Hydrochloride injection, a trusted antihypertensive therapy equivalent to the internationally recognized Trandate®. Manufactured in WHO-GMP certified facilities, Beeta-L supports advanced cardiovascular and critical care management, particularly in acute and emergency hypertension control.

Labetalol is a combined alpha- and beta-adrenergic receptor blocker that effectively reduces blood pressure by decreasing systemic vascular resistance while maintaining cardiac output. Beeta-L Injection is primarily indicated for management of severe hypertension, hypertensive emergencies, perioperative blood pressure control, and hypertension associated with pregnancy (including pre-eclampsia and eclampsia).

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Beeta-L Injection is manufactured under stringent GMP and 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 intensive care units, emergency departments, cardiology centers, maternity hospitals, 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.