Lincoln Pharmaceuticals Ltd.
Dermatological and pediatric formulations
Lincoln Pharmaceuticals is a Gujarat-based manufacturer of branded generic formulations, focusing on dermatology, pediatrics, and women's health. Its GMP-compliant facility produces tablets, capsules, creams, and injectables for domestic and semi-regulated export markets. The company exports to over 50 countries.
- Type
- Manufacturer
- Location
- Ahmedabad, India
- Founded
- 1979
- Website
- https://www.lincolnpharma.com
- Categories
- Medical & Healthcare Supplies
- Markets
- India, Bangladesh, Sri Lanka, United Arab Emirates, Kenya, Philippines
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-09 Domain registry record
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- 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)
- registry-id-verified (green), checked 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- registered-since (green), checked 1995-01-20 Company Master Data (Ministry of Corporate Affairs)
- registered-address (green), checked 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- gmp-certified (green), checked 2019-12-09 EudraGMDP, EU register of GMP certificates (EMA)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
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)