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dapagliflozin and metformin hydrochloride

NDC 67877-619 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211563
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDAPAGLIFLOZIN (5 mg/1)
METFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20260406
Package count2

External sources

Source: openFDA. Public-domain (CC0).