Aarti Drugs Ltd.
High-quality active pharmaceutical ingredients manufacturer
Aarti Drugs Ltd. manufactures active pharmaceutical ingredients, pharmaceutical intermediates, and specialty chemicals. The company operates FDA-approved and EU-GMP-compliant facilities near Mumbai and supplies to major pharmaceutical formulators worldwide. It is known for APIs in antibiotics, antifungals, and anti-inflammatory therapeutic categories.
- Type
- Manufacturer
- Location
- Mumbai, India
- Founded
- 1984
- Website
- www.aartidrugs.com
- Categories
- Medical & Healthcare Supplies
- Markets
- United States, United Kingdom, Brazil, South Africa, Egypt
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- domain-registered (green), checked 2026-08-03 Domain registry record
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- standards-mark-certified (green), checked 2026-08-21 Bureau of Indian Standards (BIS), all-India first licence report (ISI Standard Mark)
- 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)
- 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
- ISO 9001, Quality Management IAF CertSearch
- 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)