Bal Pharma is a leading Indian Pharmaceutical Company with 32+years’ of experience, specialized in Prescription Drugs, Generic medicines & OTC Products, Intravenous Infusion and Bulk Actives. We strive hard to improve the quality of life for patients by providing them products that are Safe, Effective, High Quality and Affordable. Bal Pharma’s API and FDF are produced at world class manufacturing facilities. Our APIs are largely exported to Europe, Far East, Latin America, Africa, Middle East and other World markets. The FDF are exported to Semi-Regulated, Non-Regulated market and are now foraying to regulated market. We are also one of the strong contenders for World Tender Business.
API Active Pharmaceutical Ingredients
Bal Pharma API (Active Pharmaceutical Ingredients) business began in 1996 with a simple objective of facilitating the manufacture of
niche molecules that have been able to take the benefits of vertical integration to international and domestic markets.
Bal Pharma’s API business has the competence and knowledge to undertake more than 30 different types of complex chemical
reactions. Whether these are Advance Intermediates, Fine Chemicals or Active Pharmaceuticals Ingredients, the company can
seamlessly scale up from MG to MT quantities. It offers various activities like:
Bal Pharma has a winning formula of cutting edge technology, handled by a highly qualified professional with a passion to deliver beyond
excellence. We are successfully exporting Finished Formulation to more than 40 countries. We offer extensive range of products covering dosage
forms – tablets, capsules, syrups, suspensions, IV infusions, Ophthalmic, creams and ointments to various Semi-Regulated markets. We are now
foraying into regulated markets with our new manufacturing facility in Uttaranchal, equipped with ultra modern machinery.
We offer more than 200 formulations in 20 different therapeutic segments having strong presence in Africa, SEA, CIS, Middle East and Latin
American countries.
Our manufacturing facility have got approvals from various International Regulatory Authorities including NDA Uganda, PPB Kenya, TFDA Tanzania,
NAFDAC Nigeria, SBDMA Yemen, PMPB Malawi, MCAZ Zimbabwe and MOH Sudan
- State-of-the-art Pilot and Commercial Scale multipurpose facilities
- Pharmaceutical Manufacturing Plants conforming to GMP guidelines
- R & D facilities to support early development of Generic APIs
- Patent non-infringing processes
- High quality documents – Drug master file