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Country of origin : India
None products found

rizatriptan

Tablets 5 mg, 10 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP, WHO
Manufacturer #1356
The company, established in 2005, focuses on generic pharmaceuticals, particularly in niche segments like oncology, CNS, gastroenterology, and anti-diabetics. Specializing in the development of finished formulations and product dossiers, the company prepares for upcoming patent expirations to expand its market presence. With state-of-the-art, WHO-GMP certified manufacturing facilities across the country, the company supplies high-quality formulations globally under its own license and through contract manufacturing. Committed to improving quality of life, the company emphasizes innovation and consistency in its product offerings, aiming to meet the specific needs of diverse markets worldwide.

Manufacturer usually replies in 21 days

Differentiated dosage form - Oral Disintegrating Strip

rizatriptan

Oral film 10 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #36950
European pharmaceutical company with experience in developing and commercializing specialty and generic Rx medicines for European and international markets. Oral solid, liquid, and injectable dosage forms cover key therapeutic areas. Engages in strategic licensing partnerships for product development and market expansion.

Manufacturer usually replies in 15 days

rizatriptan

Tablets 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
India
GMP approvals
EU GMP
Unavailable markets
South Africa , United Kingdom
Registered in
United States
Manufacturer #638

A pharmaceutical manufacturer producing a broad range of pharmaceutical products that include finished dosage forms such as tablets, capsules, oral liquids and other formulations for various therapeutic areas, as well as active pharmaceutical ingredients used in drug manufacture and export to global markets. The company integrates research and development with large-scale production and maintains quality systems aligned with industry standards to support safety, consistency and compliance in the development and supply of its pharmaceutical products.

Manufacturer usually replies in 91 days

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