Active Ingredient: METFORMIN HYDROCHLORIDE
Proprietary Name: METFORMIN HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB3
Application Number: A212969
Product Number: 001
Approval Date: Nov 25, 2019
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information