Intas Pharmaceuticals
Formulaciones farmacéuticas, biosimilares e inyectables.
Intas Pharmaceuticals fabrica formulaciones farmacéuticas, biosimilares e inyectables en sus operaciones de Ahmedabad. La empresa abastece a clientes minoristas, industriales, sanitarios, de servicios alimentarios o de exportación en sus principales mercados cotizados.
- Type
- brand seeking distribution
- Location
- Ahmedabad, India
- Founded
- 1977
- Website
- intaspharma.com
- Categories
- Suministros médicos y sanitarios
- Markets
- India, Estados Unidos, Reino Unido, Alemania
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- customer-reviews (amber), checked 2026-08-08 MouthShut
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registered-trade-only (amber), 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)
- registered-manufacturer (green), checked 2026-08-18 Chemistry, Food and Drugs Division, Ministry of Health of Trinidad and Tobago, register of drugs (Food and Drugs Act Chap. 30:01)
Claimed certifications
- Good Manufacturing Practice
- FDA Registered FDA Establishment Registration
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)