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Metformin hydrochloride

NDC 27241-241 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAjanta Pharma USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213962
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20210309
Package count1

External sources

Source: openFDA. Public-domain (CC0).