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Donepezil hydrochloride

NDC 55111-302 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDr. Reddys Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202723
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (23 mg/1)
Marketing started20250820
Package count2

External sources

Source: openFDA. Public-domain (CC0).