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Donepezil hydrochloride

NDC 55111-356 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDr. Reddys Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA201001
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (5 mg/1)
Marketing started20110531
Package count5

External sources

Source: openFDA. Public-domain (CC0).