Flagship Biotech International Pvt. Ltd.

1204, Rupa Solitaire, Plot A-1, Sector -1 MBP T.T.C. Indl Area Mahape

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Company Profile

Flagship Biotech International Pvt.Ltd was established in the 2009 and Headquartered in the Heart of India – Mumbai, having branch offices in western India and Global subsidiary offices in USA & Mexico. We are one of the fastest growing India’s leading Generic and Specialty Pharmaceutical companies engaged into Developing, Manufacturing and Marketing a broad range of Pharmaceutical Formulations. More than 700 pharmaceutical Formulations in various dosage forms like Solid Dosage Form - Tablets, Capsules, Dry Powder for Orals, Liquid Orals, Small Volume Parenteral (SVP), Large Volume Parenteral (LVP) & Powder for Injections, Ointment, Creams, Inhalers and Herbals are Marketed across the Globe. We believe that our competitive advantage in the International Market lies in our established presence in all major therapeutic areas including Oncology, Anti-Diabetic, Cardiology, Pain and Analgesics, Gynecology, Anti-infectives, Vitamins, Minerals, Nutrients, Gastro-Intestinal, Anti-Osteoporosis, Anti-Malarial, Immunosuppressant, Anti-Bacterial, Anti- Asthmatics, Anti-Allergy etc. Currently, Flagship Biotech International operates in more than 75 countries worldwide having more than 400 products registered. Flagship Biotech International has extensive presence in many countries in Asia, Africa and Latin America, CIS, Australia & Pacific Ocean with broad product portfolio to suit the needs of each country Our Global Participation in Government supply – IRAN, TNT, NHF, NHP, PNA,PNG, MPC The company has earned client’s and customer’s support due to its commitment and consistency in fulfilling the needs and demands. Our state of the Art Manufacturing Facilities maintaining high Quality standards at every further stage in manufacturing process are located in Tarapur near Mumbai (Maharashtra, India) Navsari, Naroda (Gujrat, India), Baddi (Himachal Pradesh, India) Manufacturing facilities comply with Quality Standards of global regulatory authorities with WHO – GMP Approval. Our R&D capabilities include Dossier Development, Chemical Synthesis, Process Optimization, Formulation Research & Development, Analytical Development and Conducting Stability Studies.