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donepezil hydrochloride

NDC 70518-1666 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA200292
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (10 mg/1)
Marketing started20181112
Package count2

External sources

Source: openFDA. Public-domain (CC0).