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Cyproterone manufacturers

14 products found

Filters

14 products found

cyproterone + ethinylestradiol

Tablets 2 mg + 0.035 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Unavailable markets
Vietnam
Manufacturer #21467

This global pharmaceutical company is dedicated to improving patients' lives through high-quality, differentiated products and services. They leverage a collaborative network to achieve success in key regions like the EU and North America. Their focus areas include women's health, infectious diseases, and potentially other therapeutic areas based on their recent approvals and launches. They produce prescription medications (including injectables) and tablets, demonstrating expertise in various dosage forms. The company holds GMP certifications and boasts successful product patents, solidifying its commitment to quality and innovation.

Manufacturer usually replies in 23 days

cyproterone

Tablets 50 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Moldova
GMP approvals
WHO
Manufacturer #17541

Manufacturer usually replies in 2 days

cyproterone + ethinylestradiol

Tablets 2 mg+0,035 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Pakistan
GMP approvals
United Kingdom
Manufacturer #18910
This pharmaceutical company, established in 1990, is a leader in its region, boasting over 180 registered products marketed both domestically and internationally. Specializing in innovative drug formulations and medicines, the company holds a prestigious MHRA CGMP certification, granting it the authority to market products within the EU and UK. Their production capabilities are extensive, reaching up to 1,000,000 units daily, thanks to advanced machinery imported from Germany, Switzerland, China, and Italy. The company's expertise spans various therapy areas, including (information not provided), utilizing principal dosage forms such as (information not provided). They offer contract manufacturing services to reputable international companies and adhere to strict GMP guidelines, evident in their product patents and registrations with the local regulatory authority (DRAP).

Manufacturer usually replies in 7 days

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