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Dapagliflozin and Metformin Hydrochloride

NDC 63304-028 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211491
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDAPAGLIFLOZIN (10 mg/1)
METFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20260406
Package count2

External sources

Source: openFDA. Public-domain (CC0).