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Donepezil Hydrochloride

NDC 16571-779 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090056
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (10 mg/1)
Marketing started20110531
Package count4

External sources

Source: openFDA. Public-domain (CC0).