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Metformin Hydrochloride

NDC 68788-7205 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078321
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (750 mg/1)
Marketing started20180723
Marketing ended20260930
Package count5

External sources

Source: openFDA. Public-domain (CC0).