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Dapagliflozin and Metformin Hydrochloride

NDC 42571-320 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211466
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDAPAGLIFLOZIN (5 mg/1)
METFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20261001
Package count3

External sources

Source: openFDA. Public-domain (CC0).