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Metformin Hydrochloride

NDC 24658-792 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPuraCap Laboratories LLC dba Blu Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA075965
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20160401
Package count1

External sources

Source: openFDA. Public-domain (CC0).