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Metformin Hydrochloride

NDC 11788-037 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameMetformin Hydrochloride Extended-Release Tablets
Labeler / ManufacturerAiPing Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209993
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20251215
Package count1

External sources

Source: openFDA. Public-domain (CC0).