Ajanta Pharma
Produits pharmaceutiques spécialisés, génériques de marque et formulations.
Ajanta Pharma fabrique des produits pharmaceutiques spécialisés, des génériques de marque et des formulations à partir de ses opérations de Mumbai. L'entreprise fournit des clients de détail, industriels, de santé, de restauration ou d'exportation sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Mumbai, India
- Founded
- 1973
- Website
- ajantapharma.com
- Categories
- Fournitures médicales et de santé
- Markets
- Inde, États-Unis, Émirats arabes unis, Afrique du Sud
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- registry-id-verified (green), checked 2026-06-04 MCA21, Ministry of Corporate Affairs
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-23 Rwanda FDA, register of registered human medicinal products
- sanctions-clear (green), checked 2026-08-04 OpenSanctions
- debarment-clear (green), checked 2026-08-04 OpenSanctions
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
Claimed certifications
- Good Manufacturing Practice
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)