Bal Pharma Ltd.
Prescription and generic pharmaceutical products
Bal Pharma manufactures a wide range of branded generics, including antibiotics, anti-diabetics, and dermatological products. Its WHO-GMP certified facility in Uttarakhand supplies formulations to emerging markets across Asia and Africa. The company focuses on affordable, niche therapeutic segments.
- Type
- Manufacturer
- Location
- Bengaluru, India
- Founded
- 1987
- Website
- https://www.balpharma.com
- Categories
- Medical & Healthcare Supplies
- Markets
- United Arab Emirates, Philippines, Kenya, Russia, Sri Lanka
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-05 Domain registry record
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-05 OpenSanctions
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-05 OpenSanctions
- customer-reviews (amber), checked 2026-08-05 MouthShut
- cin-on-site (amber), checked 2026-08-11 Published on the company's own website
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
- 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)
- registry-id-verified (green), checked 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- registered-since (green), checked 1987-05-19 Company Master Data (Ministry of Corporate Affairs)
- registered-address (green), checked 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
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)