Glenmark Pharmaceuticals
Branded generics, specialty medicines and apis.
Glenmark Pharmaceuticals manufactures branded generics, specialty medicines and APIs from its Mumbai operations. The company supplies retail, industrial, healthcare, foodservice or export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- Mumbai, India
- Founded
- 1977
- Website
- glenmarkpharma.com
- Categories
- Medical & Healthcare Supplies
- Markets
- India, United States, Germany, Brazil
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- product-authorised-for-sale (green), checked 2026-08-23 Rwanda FDA, register of registered human medicinal products
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- 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-manufacturer (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
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)