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Dapagliflozin

NDC 70954-856 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211156
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDAPAGLIFLOZIN (5 mg/1)
Marketing started20260513
Package count1

External sources

Source: openFDA. Public-domain (CC0).