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Country of origin : India
None products found

dapoxetine hydrochloride

Tablets 30 mg, 60 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #38861
India-based pharmaceutical formulations company manufacturing Rx generic oral solids, liquids, and semi-solids for domestic and regulated export markets. Dosage forms span infections, metabolic, and cardiovascular therapy areas aligned with Indian and international GMP standards. Committed to quality manufacturing and compliance for multi-market pharmaceutical distribution.

Manufacturer usually replies in 84 days

dapoxetine hydrochloride

Tablets 30 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #19639

This globally operating pharmaceutical company focuses on developing and manufacturing a broad range of affordable medications. They specialize in both prescription and over-the-counter drugs, including oncology treatments, antibacterials, injectables (both specialty and large volume), ophthalmic products, dermatological preparations, and veterinary pharmaceuticals. Their product portfolio also includes unique niche drugs and orphan products, showcasing their commitment to addressing diverse medical needs. The company boasts state-of-the-art manufacturing facilities located across several regions, adhering to strict quality standards recognized by international regulatory bodies like the WHO GMP, US FDA, and MCC. Their extensive global reach spans over 45 countries in Asia, Africa, Latin America, CIS, Europe, Australia, and the Pacific Ocean. The company's focus on research and development, coupled with its global manufacturing capabilities and commitment to quality, positions them as a key player in the international pharmaceutical market.

Manufacturer usually replies in 21 days

vardenafil + dapoxetine hydrochloride

Tablets 20 mg + 60 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #34549

Established in 2016, this WHO-GMP certified manufacturer specializes in the production and export of pharmaceutical, nutraceutical, and ayurvedic products, including tablets, capsules, syrups, and injections. As a CTD dossier owner and manufacturer, it ensures compliance with international quality standards. The company operates state-of-the-art manufacturing facilities adhering to stringent GMP guidelines. Its products are distributed across multiple countries worldwide, with registrations in regions such as the Dominican Republic, Philippines, Myanmar, Uzbekistan, Turkmenistan, Iraq, and Kuwait. 

 

Manufacturer usually replies in 15 days

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