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Country of origin : India
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hydrocortisone sodium succinate

Powder for solution for injection 25 mg, 100 mg, 500 mg, 1000 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #35915

Established in 2007, this family-owned manufacturer specializes in pharmaceutical formulations, offering over 500 products across various dosage forms, including tablets, capsules, dry syrups, ointments, dry injections, and liquid orals. As a CTD dossier owner and manufacturer, it holds WHO-cGMP certification, ensuring compliance with stringent international quality standards. The manufacturer operates advanced production lines with capacities such as 3,600 million tablets, 1,800 million capsules, 240 million liquid injections in ampoules, and 70 million dry powder injections per annum, adhering to rigorous GMP guidelines. As a CTD dossier owner and manufacturer, its products are distributed across multiple countries worldwide.

Manufacturer usually replies in 13 days

hydrocortisone sodium succinate

Injection 100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
Uzbekistan, Libya, Congo, Tanzania, Uganda, Phillipines, Kuwait, Ghana, Nigeria, Kenya, Azerbaijan, Peru, WHO
Manufacturer #38905
Indian pharmaceutical company manufacturing generic Rx oral solid and liquid formulations across essential therapy areas for domestic and international markets. Quality-driven production is aligned with domestic GMP standards and targeted export market regulatory requirements. Serves emerging markets with a diverse and affordable generic medicines portfolio.

Manufacturer usually replies in 6 days

hydrocortisone sodium succinate

Injection 100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP, ANVISA, INVIMA
Manufacturer #11735
Indian pharmaceutical manufacturer established in the 1980s with over four decades of experience producing Rx tablets, capsules, oral liquids, ointments, and eye drops. Exports to 80+ countries across Asia, Africa, Latin America, and CIS markets. Holds WHO-GMP, EU-GMP, PIC/s, ANVISA, COFEPRIS, and DIGEMID regulatory approvals.

Manufacturer usually replies in 26 days

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