One of the core business areas of Cadila Pharmaceuticals is to synthesize Active Pharmaceutical Ingredients APIs of the highest standard in an integrated cost effective manner. Spread over 80, 000 square meter area, ISO-9001 & ISO14001 API manufacturing facility at Ankleshwar, India is accredited by USFDA, EDQM European Directorate of Quality Medicine, AIFA Agenzia Italiana del Farmaco, TGA Theapeutic Goods Administration, Australia and WHO. The company offers more than 38 APIs and intermediates which are exported across the world. Having filed 29 USDMFs, CEP for 09 APIs and with more in pipeline, the unit is committed to offer an unmatched portfolio.