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menotrophin

Injection 75 IU, 150 IU, 600 IU, 900 IU, 1200 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Unavailable markets
Iraq
Manufacturer #23023

Established in 2008, the manufacturer excels as a CTD dossier owner and manufacturer, distributing its pharmaceutical products across multiple countries. Renowned as a GMP manufacturer, it employs state-of-the-art production lines specifically designed to meet stringent quality standards, essential for a CTD dossier owner and manufacturer. This underscores their commitment to excellence and safety in drug manufacturing, ensuring they maintain their status as a leading CTD dossier owner and manufacturer.

 

 

 

 

Manufacturer usually replies in 6 days

menotrophin

Powder for solution for injection 75 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Egypt
GMP approvals
WHO
Manufacturer #16472
This pharmaceutical company, based in the Middle East, has been operating for over four decades. With a focus on production, they are a leading manufacturer in the region, particularly known for their antibiotics, lyophilized products, and spansule capsules. They hold significant market share in the local market and boast the number one spot in pharmaceutical product exports. They offer a wide range of prescription drugs, including those in solid, injectable, oral, and liquid forms. The company has obtained EU and US GMP approvals, indicating adherence to high manufacturing standards. Their production lines encompass various therapeutic areas, with key focuses on antibiotics, oncology, and cardiology. While no specific product patents were mentioned, their commitment to research and development suggests an ongoing effort to innovate and expand their offerings.

Manufacturer usually replies in 62 days

menotrophin

Vials, lyophilized 75 IU, 150 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #10170
A pharmaceutical manufacturer providing export-oriented development and commercial supply of pharmaceutical products across a complete range of finished dosage forms, including tablets, capsules, softgels, injectables, ointments, dry syrups, and sachet presentations. The organisation positions itself as a licensing-and-supply partner with integrated manufacturing expertise and a growing international portfolio, and it reports holding multiple regulatory approvals from major global authorities (including MHRA, TGA, ANVISA and GCC regulators) alongside WHO-GMP compliance for its manufacturing operations, supporting consistent quality and reliability of pharmaceutical products for overseas partners.

Manufacturer usually replies in 27 days

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