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Donepezil Hydrochloride

NDC 71205-948 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203104
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (23 mg/1)
Marketing started20150301
Package count5

External sources

Source: openFDA. Public-domain (CC0).