Unnati Pharmax

Apiedge 5mg Tablets
Composition: Apixaban 5mg
International Trade Name: Eliquis®

Apiedge 5mg Tablets are a high-quality Apixaban 5mg oral formulation, a therapeutic equivalent of the internationally recognized direct oral anticoagulant (DOAC) marketed under the brand name Eliquis®. Manufactured in WHO-GMP certified facilities, Apiedge Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global cardiology and thromboembolic care programs.

Apixaban is a selective and reversible factor Xa inhibitor that prevents the conversion of prothrombin to thrombin, thereby reducing clot formation in the circulatory system. This targeted mechanism provides effective anticoagulation with a predictable pharmacokinetic profile, minimizing the risk of stroke, systemic embolism, and venous thromboembolism.

Apiedge 5mg Tablets are primarily indicated for the prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation, treatment and prevention of deep vein thrombosis (DVT), pulmonary embolism (PE), and for patients at risk of thromboembolic complications following surgery.

Apiedge 5mg Tablets are manufactured under stringent GMP and pharmaceutical 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 clinics, hospitals, tertiary care facilities, government healthcare programs, and international pharmaceutical distributors.

Albucel 20% Solution
Composition: Human Albumin 20%
International Trade Name: Albucel®

Albucel 20% Solution is a high-quality Human Albumin 20% formulation, a therapeutic plasma protein product designed to restore and maintain plasma volume, colloid osmotic pressure, and protein levels in patients requiring albumin therapy. Manufactured in WHO-GMP certified facilities, Albucel 20% is supplied by trusted pharmaceutical exporters from India to support advanced global critical care, surgery, and plasma replacement programs.

Human albumin is a naturally occurring plasma protein that maintains oncotic pressure, transports endogenous and exogenous substances, and supports overall circulatory stability. Albucel 20% Solution provides rapid and effective plasma volume expansion, supporting patient management in hypovolemia, hypoalbuminemia, burns, shock, and other critical conditions.

Albucel 20% Solution is primarily indicated for hypovolemic shock, hypoalbuminemia, burns, acute liver failure, nephrotic syndrome, and perioperative plasma volume support during surgery or cardiopulmonary bypass. It is administered under specialist supervision in hospital and critical care settings.

Albucel 20% Solution is manufactured under stringent GMP and plasma fractionation quality standards, ensuring consistent purity, safety, and stability. The solution is supplied in secure, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, intensive care units, government health programs, and international pharmaceutical distributors.

ALBU-H – Human Normal Albumin 20% / 25%
Composition: Human Normal Albumin
International Trade Name: ALBU-H®

ALBU-H is a high-quality Human Normal Albumin solution, a therapeutic plasma protein product designed to restore and maintain plasma volume, oncotic pressure, and protein levels in patients requiring albumin therapy. Manufactured in WHO-GMP certified facilities, ALBU-H is supplied by trusted pharmaceutical exporters from India to support advanced global critical care, surgery, and plasma replacement programs.

Human albumin is a naturally occurring plasma protein that helps maintain colloid osmotic pressure, transport endogenous and exogenous substances, and support overall circulatory stability. ALBU-H provides rapid and effective plasma volume expansion, aiding in the management of hypovolemia, hypoalbuminemia, burns, shock, and other critical conditions.

ALBU-H is primarily indicated for hypovolemic shock, hypoalbuminemia, burns, acute liver failure, nephrotic syndrome, and during cardiopulmonary bypass or surgical procedures requiring plasma volume support. It is administered under specialist supervision in hospital and critical care settings.

ALBU-H is manufactured under stringent GMP and plasma fractionation quality standards, ensuring consistent purity, safety, and stability. The solution is supplied in secure, cold-chain compliant, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, intensive care units, government health programs, and international pharmaceutical distributors.

KILLPREG Tablets
Composition: Mifepristone Tablets + Misoprostol Tablets
International Trade Reference: Mifeprex® + Cytotec®

KILLPREG is a high-quality combination pack of Mifepristone and Misoprostol tablets, formulated to provide a reliable and clinically validated medical termination solution. Manufactured in WHO-GMP certified facilities, KILLPREG is supplied by trusted pharmaceutical exporters from India to support global reproductive health and gynecology care programs.

Mifepristone is a progesterone receptor antagonist that works by blocking the hormone progesterone, which is essential for the continuation of pregnancy. Misoprostol is a prostaglandin analog that induces uterine contractions, leading to the expulsion of the pregnancy tissue. Together, this combination offers a non-surgical, effective, and widely accepted method for medical abortion under appropriate medical supervision.

KILLPREG is primarily indicated for the medical termination of early intrauterine pregnancy, management of missed abortion, and certain gynecological conditions as prescribed by qualified healthcare professionals. The combination is globally recognized for its safety, efficacy, and predictable clinical outcomes when used according to approved medical guidelines.

KILLPREG Tablets are manufactured under stringent GMP and pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, gynecology clinics, women’s health centers, government healthcare programs, NGOs, and international pharmaceutical distributors.

Cytoheal 200 Tablets
Composition: Misoprostol 200mcg
International Trade Name: Cytotec®

Cytoheal 200 is a high-quality Misoprostol 200mcg Tablet, a therapeutic equivalent of the internationally recognized prostaglandin E1 analog marketed under the brand name Cytotec®. Manufactured in WHO-GMP certified facilities, Cytoheal Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global gynecology, obstetrics, and gastroenterology treatment programs.

Misoprostol is a synthetic prostaglandin E1 analog that exerts cytoprotective effects on the gastric mucosa and induces uterine contractions by acting on smooth muscle fibers. This dual mechanism makes Cytoheal 200 effective in the prevention of NSAID-induced gastric ulcers and in various gynecological and obstetric applications.

Cytoheal 200 Tablets are primarily indicated for the prevention and treatment of gastric ulcers, medical termination of pregnancy (under medical supervision), induction of labor, management of postpartum hemorrhage, and cervical ripening in obstetric procedures.

Cytoheal 200 Tablets are manufactured under stringent GMP and pharmaceutical 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, maternity centers, gynecology clinics, government health programs, and international pharmaceutical distributors.

Progynova 2mg Tablets
Composition: Estradiol Valerate 2mg
International Trade Name: Progynova®

Progynova 2mg is a high-quality Estradiol Valerate 2mg Tablet, a therapeutic equivalent of the internationally recognized estrogen replacement therapy marketed under the brand name Progynova®. Manufactured in WHO-GMP certified facilities, Progynova Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global gynecology and endocrinology treatment programs.

Estradiol valerate is a prodrug of estradiol, a natural estrogen, which is converted in the body to active estradiol. It helps restore and maintain normal estrogen levels, supporting the regulation of menstrual cycles, maintenance of secondary sexual characteristics, and overall reproductive and bone health. This targeted hormonal action helps alleviate symptoms associated with estrogen deficiency.

Progynova 2mg Tablets are primarily indicated for hormone replacement therapy (HRT) in women with estrogen deficiency, including the management of menopausal symptoms such as hot flushes, night sweats, vaginal dryness, and mood changes. It is also used in the treatment of menstrual disorders, ovarian failure, and as part of assisted reproductive protocols under medical supervision.

Progynova 2mg Tablets are manufactured under stringent GMP and pharmaceutical 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, fertility centers, hospitals, government healthcare programs, and international pharmaceutical distributors.

AlbuSun Injection
Composition: Human Albumin 20% / 25% (depending on formulation)
International Trade Name: AlbuSun®

AlbuSun is a high-quality Human Albumin Solution, a therapeutic equivalent of the internationally recognized plasma-derived albumin preparations used in critical care, surgery, and hematology. Manufactured in WHO-GMP certified facilities, AlbuSun Injection is supplied by trusted pharmaceutical exporters from India to support advanced global healthcare, intensive care, and plasma therapy programs.

Human Albumin is a natural plasma protein that plays a vital role in maintaining oncotic pressure, fluid balance, and transport of hormones, drugs, and endogenous substances. AlbuSun Injection provides rapid plasma volume expansion, supports hemodynamic stability, and replenishes protein levels in patients with hypoalbuminemia or blood loss.

AlbuSun Injection is primarily indicated for the treatment of hypovolemia, hypoalbuminemia, shock, burns, major surgery, liver cirrhosis with ascites, nephrotic syndrome, and other conditions requiring plasma volume expansion or protein replacement therapy.

AlbuSun 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 hospitals, intensive care units, tertiary care facilities, government healthcare programs, and international pharmaceutical distributors.

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Unnati Pharmax, a reputable pharmaceutical company, recognized the evolving needs of the healthcare industry and embraced innovation by offering medicine drop shipping services. This approach allows individuals and businesses to access a wide range of medications and healthcare products conveniently, irrespective of their location.

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Aprelieva Capsules
Composition: Aprepitant 125mg / 80mg
International Trade Name: Emend®

Aprelieva is a high-quality Aprepitant capsule formulation, a therapeutic equivalent of the internationally recognized neurokinin-1 (NK1) receptor antagonist marketed under the brand name Emend®. Manufactured in WHO-GMP certified facilities, Aprelieva Capsules are supplied by trusted pharmaceutical exporters from India to support advanced global oncology supportive care programs.

Aprepitant is a selective NK1 receptor antagonist that blocks the action of substance P in the central nervous system, a key mediator of nausea and vomiting. This targeted mechanism helps prevent both acute and delayed chemotherapy-induced nausea and vomiting (CINV), significantly improving patient comfort and treatment adherence during cancer therapy.

Aprelieva Capsules are primarily indicated for the prevention of acute and delayed nausea and vomiting associated with highly emetogenic and moderately emetogenic chemotherapy regimens. It is commonly used in combination with other antiemetic agents such as serotonin (5-HT3) antagonists and corticosteroids for enhanced protection.

Aprelieva Capsules are manufactured under stringent GMP and pharmaceutical 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 oncology centers, tertiary care hospitals, chemotherapy units, government cancer programs, and international pharmaceutical distributors.

Distinon 60mg Tablets
Composition: Pyridostigmine 60mg
International Trade Name: Mestinon®, Regonol®, Gravitor®

Distinon 60mg is a high-quality Pyridostigmine 60mg tablet, a therapeutic equivalent of the internationally recognized cholinesterase inhibitor marketed under the brand names Mestinon®, Regonol®, and Gravitor®. Manufactured in WHO-GMP certified facilities, Distinon Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global neurology and myasthenia gravis management programs.

Pyridostigmine acts by inhibiting acetylcholinesterase, thereby increasing the concentration of acetylcholine at neuromuscular junctions. This mechanism improves muscle strength and reduces fatigue in patients with neuromuscular disorders, particularly myasthenia gravis.

Distinon 60mg Tablets are primarily indicated for the symptomatic treatment of myasthenia gravis, postoperative or drug-induced neuromuscular blockade, and other conditions requiring enhancement of cholinergic transmission under specialist supervision.

Distinon 60mg Tablets are manufactured under stringent GMP and pharmaceutical 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 neurology clinics, hospitals, tertiary care centers, government health programs, and international pharmaceutical distributors.

APRELIEVA 125mg Capsules
Composition: Aprepitant 125mg
International Trade Name: Emend®

APRELIEVA 125mg is a high-quality Aprepitant 125mg Capsule, a therapeutic equivalent of the internationally recognized neurokinin-1 (NK1) receptor antagonist marketed under the brand name Emend®. Manufactured in WHO-GMP certified facilities, APRELIEVA Capsules are supplied by trusted pharmaceutical exporters from India to support advanced global oncology and supportive care treatment programs.

Aprepitant selectively blocks the NK1 receptor in the central nervous system, inhibiting the action of substance P, a key mediator of nausea and vomiting. This targeted mechanism makes APRELIEVA 125mg Capsules highly effective in preventing chemotherapy-induced nausea and vomiting (CINV), especially when used as part of combination antiemetic regimens.

APRELIEVA 125mg Capsules are primarily indicated for the prevention of acute and delayed nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy. It is commonly used in combination with a 5-HT3 antagonist and a corticosteroid to enhance antiemetic protection.

APRELIEVA 125mg Capsules are manufactured under stringent GMP and pharmaceutical 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 oncology centers, tertiary care hospitals, chemotherapy units, government cancer programs, and international pharmaceutical distributors.

Ironup 1000mg Injection
Composition: Ferric Carboxymaltose Injection 1000mg
International Trade Name: Injectafer® / Ferinject®

Ironup 1000mg is a high-quality Ferric Carboxymaltose 1000mg Injection, a therapeutic equivalent of the internationally recognized intravenous iron formulation marketed under the brand names Injectafer® and Ferinject®. Manufactured in WHO-GMP certified facilities, Ironup Injection is supplied by trusted pharmaceutical exporters from India to support advanced global hematology and critical care treatment programs.

Ferric carboxymaltose is a stable iron complex that enables controlled and targeted delivery of iron directly into the bloodstream, allowing rapid replenishment of iron stores with minimal gastrointestinal side effects. This formulation supports efficient hemoglobin synthesis, improves oxygen transport, and restores normal iron levels in patients with moderate to severe iron deficiency.

Ironup 1000mg Injection is primarily indicated for the treatment of iron deficiency anemia in adults and children, especially in cases where oral iron therapy is ineffective, poorly tolerated, or unsuitable. It is widely used in patients with chronic kidney disease, inflammatory bowel disease, postpartum anemia, heavy menstrual bleeding, and perioperative anemia management.

Ironup 1000mg Injection is manufactured under stringent GMP and pharmaceutical 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 hospitals, dialysis centers, maternity units, tertiary care facilities, government health programs, and international pharmaceutical distributors.

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

Paxzen Tablets are a high-quality combination of Nirmatrelvir and Ritonavir, a therapeutic equivalent of the internationally recognized antiviral therapy marketed under the brand name Paxlovid®. Manufactured in WHO-GMP certified facilities, Paxzen Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global infectious disease and COVID-19 treatment programs.

Nirmatrelvir is a SARS-CoV-2 main protease inhibitor that prevents viral replication by blocking the processing of viral polyproteins, while Ritonavir acts as a pharmacokinetic enhancer by slowing the metabolism of Nirmatrelvir, ensuring sustained plasma concentrations for optimal antiviral efficacy. This combination provides a targeted oral therapy for early-stage COVID-19 infections.

Paxzen Tablets are primarily indicated for the treatment of mild-to-moderate COVID-19 in adult and pediatric patients at high risk of progression to severe disease, hospitalization, or death. The therapy is most effective when administered as soon as possible after diagnosis and within recommended clinical guidelines.

Paxzen Tablets are manufactured under stringent GMP and pharmaceutical 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, COVID-19 care centers, government health programs, telemedicine providers, and international pharmaceutical distributors.

IMMUGL Injection
Composition: Human Normal Immunoglobulin (IVIG)
International Trade Name: Intravenous Immunoglobulin (IVIG)

IMMUGL is a high-quality Human Normal Immunoglobulin Injection, a therapeutic equivalent of the internationally recognized intravenous immunoglobulin (IVIG) preparations used in immunodeficiency and autoimmune disorders. Manufactured in WHO-GMP certified facilities, IMMUGL is supplied by trusted pharmaceutical exporters from India to support advanced global immunology, neurology, and critical care treatment programs.

Human Normal Immunoglobulin is a sterile, purified preparation of polyvalent IgG antibodies derived from pooled human plasma. It provides passive immunity by neutralizing pathogens, modulating immune responses, and restoring antibody levels in patients with primary and secondary immunodeficiency states. This targeted immunomodulatory action also makes it effective in several autoimmune and inflammatory conditions.

IMMUGL is primarily indicated for the treatment of primary immunodeficiency disorders, secondary immunodeficiencies, immune thrombocytopenic purpura (ITP), Guillain-Barré syndrome, Kawasaki disease, chronic inflammatory demyelinating polyneuropathy (CIDP), and other autoimmune or inflammatory conditions where immunoglobulin therapy is recommended.

IMMUGL 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 hospitals, neurology and immunology centers, tertiary care facilities, government healthcare programs, and international pharmaceutical distributors.

U Tryp 100,000 IU Injection
Composition: Ulinastatin 100,000 IU
International Trade Name: Ulinast®

U Tryp 100,000 IU is a high-quality Ulinastatin 100,000 IU Injection, a therapeutic equivalent of the internationally recognized serine protease inhibitor marketed under the brand name Ulinast®. Manufactured in WHO-GMP certified facilities, U Tryp Injection is supplied by trusted pharmaceutical exporters from India to support advanced global critical care, inflammatory, and organ protection programs.

Ulinastatin is a broad-spectrum protease inhibitor that regulates inflammatory responses, stabilizes cell membranes, and protects organs from enzyme-mediated damage. Its targeted mechanism helps reduce systemic inflammation, prevent multiple organ dysfunction, and improve clinical outcomes in patients with severe inflammatory conditions.

U Tryp 100,000 IU Injection is primarily indicated for the management of acute pancreatitis, systemic inflammatory response syndrome (SIRS), sepsis, multiple organ dysfunction syndrome (MODS), and other conditions associated with excessive protease activity and inflammation under specialist supervision.

U Tryp 100,000 IU Injection is manufactured under stringent GMP and pharmaceutical 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 critical care units, tertiary care hospitals, government health programs, and international pharmaceutical distributors.

Covilife QTN 250 Capsules
Composition: Coenzyme Q10 250mg
International Trade Name: Covilife®

Covilife QTN 250 is a high-quality Coenzyme Q10 250mg capsule formulation, designed to support cardiovascular health, energy metabolism, and antioxidant defense. Manufactured in WHO-GMP certified facilities, Covilife QTN Capsules are supplied by trusted pharmaceutical exporters from India to support global health, wellness, and nutritional programs.

Coenzyme Q10 (CoQ10) is a naturally occurring antioxidant that plays a vital role in mitochondrial energy production and protects cells from oxidative stress. Covilife QTN 250 Capsules help maintain heart function, enhance cellular energy levels, and support overall vitality, particularly in individuals with age-related decline or increased oxidative stress.

Covilife QTN 250 Capsules are primarily indicated as a dietary supplement to support cardiovascular health, energy metabolism, and antioxidant protection. It is suitable for adults seeking to maintain heart health, improve energy levels, or support general wellness.

Covilife QTN 250 Capsules are manufactured under stringent GMP and pharmaceutical 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 pharmacies, wellness centers, hospitals, government health programs, and international pharmaceutical distributors.

Arcovit Injection
Composition: Vitamin C (Ascorbic Acid) Injection
International Trade Name: Vitamin C Injection

Arcovit is a high-quality Vitamin C (Ascorbic Acid) Injection formulated to support advanced clinical nutrition, immunity enhancement, and antioxidant therapy. Manufactured in WHO-GMP certified facilities, Arcovit Injection is supplied by trusted pharmaceutical exporters from India to support global healthcare and wellness programs.

Vitamin C is an essential water-soluble vitamin and a powerful antioxidant that plays a vital role in collagen synthesis, wound healing, immune function, and protection against oxidative stress. Arcovit Injection provides rapid and effective replenishment of Vitamin C levels in patients with deficiency or increased physiological demand, ensuring optimal cellular function and recovery.

Arcovit Injection is primarily indicated for the treatment and prevention of Vitamin C deficiency (scurvy), enhancement of immune response, support in acute infections, postoperative recovery, wound healing, and as an adjunct therapy in various medical conditions requiring antioxidant support.

Arcovit Injection is manufactured under stringent GMP and pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, export-grade packaging with complete regulatory documentation, making it suitable for hospitals, clinics, critical care units, wellness centers, government healthcare programs, and international pharmaceutical distributors.

Danocrine 200mg Capsules
Composition: Danazol 200mg
International Trade Name: Danocrine®

Danocrine 200mg is a high-quality Danazol 200mg capsule formulation, a therapeutic equivalent of the internationally recognized synthetic androgen derivative marketed under the brand name Danocrine®. Manufactured in WHO-GMP certified facilities, Danocrine Capsules are supplied by trusted pharmaceutical exporters from India to support advanced global gynecology, endocrinology, and immunology treatment programs.

Danazol is a synthetic steroid that suppresses the pituitary-ovarian axis, reducing the production of gonadotropins and ovarian hormones. This mechanism helps in the management of hormone-dependent conditions by creating a hypoestrogenic and hyperandrogenic environment, thereby alleviating symptoms and slowing disease progression.

Danocrine 200mg Capsules are primarily indicated for the treatment of endometriosis, fibrocystic breast disease, and hereditary angioedema. It is also used in certain cases of menorrhagia and other estrogen-dependent disorders under specialist supervision.

Danocrine 200mg Capsules are manufactured under stringent GMP and pharmaceutical 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 gynecology clinics, specialty care centers, tertiary care hospitals, government healthcare programs, and international pharmaceutical distributors.

Diane 35 Tablets
Composition: Cyproterone Acetate + Ethinyl Estradiol
International Trade Name: Diane-35®

Diane 35 is a high-quality combination oral hormonal tablet containing Cyproterone Acetate and Ethinyl Estradiol, a therapeutic equivalent of the internationally recognized anti-androgen and estrogen-progestin formulation marketed under the brand name Diane-35®. Manufactured in WHO-GMP certified facilities, Diane 35 Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global gynecology, dermatology, and endocrinology treatment programs.

Cyproterone acetate is a potent anti-androgen that blocks the action of male hormones (androgens), while ethinyl estradiol is a synthetic estrogen that regulates hormonal balance and stabilizes the menstrual cycle. This dual-action mechanism helps reduce androgen-related symptoms such as severe acne, hirsutism, seborrhea, and androgenic alopecia, while also providing effective contraceptive protection.

Diane 35 Tablets are primarily indicated for the treatment of androgen-dependent conditions in women, including severe acne, hirsutism, and polycystic ovary syndrome (PCOS), especially when associated with hormonal imbalance. It is also used as an oral contraceptive under medical supervision.

Diane 35 Tablets are manufactured under stringent GMP and pharmaceutical 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, dermatology centers, tertiary care hospitals, government healthcare programs, and international pharmaceutical distributors.

TEMOXYRA 20mg Tablets
Composition: Tamoxifen Citrate Tablets IP 20mg
International Trade Name: Nolvadex®

TEMOXYRA 20mg is a high-quality Tamoxifen Citrate 20mg tablet formulation, a therapeutic equivalent of the internationally recognized selective estrogen receptor modulator (SERM) marketed under the brand name Nolvadex®. Manufactured in WHO-GMP certified facilities, TEMOXYRA Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in hormone receptor–positive breast cancer.

Tamoxifen acts by selectively binding to estrogen receptors, thereby blocking the stimulatory effects of estrogen on breast cancer cells. This targeted hormonal mechanism helps inhibit tumor growth and reduces the risk of recurrence, making TEMOXYRA 20mg Tablets a cornerstone therapy in both early-stage and advanced breast cancer management.

TEMOXYRA 20mg Tablets are primarily indicated for the treatment of estrogen receptor–positive (ER+) breast cancer in both premenopausal and postmenopausal women. It is also used for the prevention of breast cancer in high-risk patients and in the treatment of metastatic breast cancer under specialist supervision.

TEMOXYRA 20mg Tablets are manufactured under stringent GMP and pharmaceutical 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 oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

GESTLIEVA 200mg Capsules
Composition: Progesterone 200mg
International Trade Name: GESTLIEVA®

GESTLIEVA 200mg is a high-quality Progesterone 200mg capsule formulation, a therapeutic equivalent of the internationally recognized natural progesterone therapy. Manufactured in WHO-GMP certified facilities, GESTLIEVA Capsules are supplied by trusted pharmaceutical exporters from India to support advanced global gynecology, reproductive health, and hormone therapy programs.

Progesterone is a naturally occurring steroid hormone that regulates the menstrual cycle, supports implantation and maintenance of pregnancy, and balances the effects of estrogen in the body. GESTLIEVA 200mg helps restore hormonal balance, support fertility, and manage conditions associated with progesterone deficiency.

GESTLIEVA 200mg Capsules are primarily indicated for the treatment of luteal phase deficiency, assisted reproductive therapy (ART), prevention of preterm birth in high-risk pregnancies, management of menstrual irregularities, and support of early pregnancy under specialist supervision.

GESTLIEVA 200mg Capsules are manufactured under stringent GMP and pharmaceutical 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 gynecology and fertility clinics, tertiary care hospitals, government healthcare programs, and international pharmaceutical distributors.

Femilon Tablets
Composition: Desogestrel + Ethinyl Estradiol
International Trade Name: Marvelon® / Femilon®

Femilon is a high-quality combination oral contraceptive tablet containing Desogestrel and Ethinyl Estradiol, a therapeutic equivalent of the internationally recognized hormonal contraceptive formulations marketed under brands such as Marvelon®. Manufactured in WHO-GMP certified facilities, Femilon Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global gynecology and reproductive health programs.

Desogestrel is a third-generation progestin that provides effective ovulation inhibition with improved cycle control, while ethinyl estradiol is a synthetic estrogen that stabilizes the endometrial lining and regulates menstrual cycles. This balanced hormonal combination ensures reliable contraception, predictable menstrual cycles, and reduced androgen-related side effects.

Femilon Tablets are primarily indicated for oral contraception in women of reproductive age. They are also used for menstrual cycle regulation, management of dysmenorrhea, and treatment of hormonal imbalance–related symptoms such as acne and irregular periods, under medical supervision.

Femilon Tablets are manufactured under stringent GMP and pharmaceutical 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, family planning centers, hospitals, government health programs, and international pharmaceutical distributors.

Himalaya Party Smart Capsules
Composition: Herbal Formulation (Natural plant-based extracts)
International Trade Name: Party Smart®

Himalaya Party Smart Capsules are a high-quality herbal formulation developed to support the body’s natural detoxification processes and promote overall wellness. Manufactured in WHO-GMP certified facilities, Party Smart Capsules are supplied by trusted herbal and nutraceutical exporters from India to support advanced global wellness and lifestyle health programs.

This unique herbal blend is formulated to support liver function, enhance metabolic detoxification, and help reduce discomfort associated with occasional overindulgence. By promoting natural cleansing mechanisms, Party Smart Capsules help maintain energy levels, mental clarity, and overall well-being.

Himalaya Party Smart Capsules are primarily indicated for individuals seeking natural support for liver health, detoxification, and general wellness, especially after dietary or lifestyle excesses. They are suitable for use as a wellness supplement under recommended guidelines.

Himalaya Party Smart Capsules are manufactured under stringent GMP and herbal 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 wellness centers, pharmacies, lifestyle clinics, e-commerce platforms, and international nutraceutical distributors.

Menopace Capsules
Composition: Multivitamins, Minerals, and Herbal Nutrients (Formulated for Menopausal Support)
International Trade Name: Menopace®

Menopace Capsules are a high-quality multinutrient formulation designed to support women’s health during the menopausal transition. Manufactured in WHO-GMP certified facilities, Menopace Capsules are supplied by trusted pharmaceutical exporters from India to support global women’s wellness and nutritional supplementation programs.

Menopace provides essential vitamins, minerals, and targeted nutrients that help maintain bone health, hormonal balance, cardiovascular function, and overall vitality. Its carefully designed formulation helps reduce symptoms associated with menopause such as fatigue, mood changes, hot flashes, and decreased energy.

Menopace Capsules are primarily indicated for nutritional supplementation in peri-menopausal and post-menopausal women, particularly those at risk of micronutrient deficiencies, reduced bone density, or general fatigue. It can be used as part of a daily wellness regimen under specialist or physician guidance.

Menopace Capsules are manufactured under stringent GMP and pharmaceutical 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 pharmacies, wellness centers, tertiary care hospitals, government health programs, and international pharmaceutical distributors.

Aprelieva Capsules
Composition: Aprepitant
International Trade Name: Emend®

Aprelieva is a high-quality Aprepitant capsule formulation, a therapeutic equivalent of the internationally recognized neurokinin-1 (NK1) receptor antagonist marketed under the brand name Emend®. Manufactured in WHO-GMP certified facilities, Aprelieva Capsules are supplied by trusted pharmaceutical exporters from India to support advanced global oncology supportive care programs.

Aprepitant is a selective NK1 receptor antagonist that blocks the action of substance P in the central nervous system, a key mediator of nausea and vomiting. This targeted mechanism helps prevent both acute and delayed chemotherapy-induced nausea and vomiting (CINV), significantly improving patient comfort, treatment adherence, and overall quality of life during cancer therapy.

Aprelieva Capsules are primarily indicated for the prevention of acute and delayed nausea and vomiting associated with highly emetogenic and moderately emetogenic chemotherapy regimens. It is commonly administered in combination with serotonin (5-HT3) receptor antagonists and corticosteroids for enhanced antiemetic protection.

Aprelieva Capsules are manufactured under stringent GMP and pharmaceutical 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 oncology centers, chemotherapy units, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.