Company Profile

The Company has three separate dedicated blocks for lyophilisation and crystalline facility for manufacturing sterile API’s and finished products. Site 1(ANVISA,Mexico & WHO GMP approved): Sterile Lyophilised PPI’s, General Lyophilised API & Vials, Dry powder Vials, site is ready for EU-GMP inspections. Site 2 (WHO GMP approved): Sterile Penicillin’s & Penems. We are having annual production capacity of Lyophilized and Crystalline Sterile API’s is of 360 MT and 24 Million Vials (6 million lyophilized vials & 18 million dry powder vials ) of Formulations finished dosage. CONTRACT MANUFACTURING FACILITY AS PER EU-GMP STANDARD AVAILABLE FOR LYOPHILISED / DRY POWDER / LIQUID VIALS