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Methylergometrine maleate manufacturers

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methylergometrine maleate

Solution for injection 0.2 mg/1 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP, Greece
Available for
Distribution only
Comments
Product is not available for Europe
Manufacturer #298

This company is a global pharmaceutical and commercial organization that has been operating for over five decades. It specializes in injectable and prescription drug products, medical devices, and food supplements. Their manufacturing facilities are EU and US GMP approved. They have a strong presence in international markets, especially in Europe, North America, and Asia. The company also prides itself on its commitment to research and development of new products, particularly in the field of monoclonal antibodies. This commitment has earned them recognition and awards for their innovation and manufacturing excellence.

Manufacturer usually replies in 8 days

methylergometrine maleate

Tablets, immediate release (IR) 0.2 mg

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
FDA
Comments
Manufacturing Unit : GPI Regulated and Sold : Rx
Manufacturer #7499
Vertically integrated pharmaceutical manufacturer with four decades of experience producing high-volume Rx and OTC APIs, formulation intermediates, and finished tablets, capsules, and sachets. Core portfolio includes analgesics, anti-diabetics, and cardiovascular products spanning paracetamol, metformin, and ibuprofen. US FDA and EU-GMP approved facilities supply North America and Europe.

Manufacturer usually replies in 27 days

methylergometrine maleate

Injection 0.2 mg/ml - 1 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #2303
A pharmaceutical manufacturer with over 25 years of experience that develops and produces fixed-dose and single-entity generic and specialty pharmaceutical products. The company offers an extensive range of injectable dosage forms, including parenterals, and also manufactures oral solids. Its facilities operate under recognised international quality certifications such as EU-GMP, ANVISA, PIC/S and TGA approvals, supporting reliable large-scale production of pharmaceutical products for global export while emphasizing efficacy, affordability and consistent quality.

Manufacturer usually replies in 20 days

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