FDA NDC Directory · JSON-LD · Markdown

Donepezil Hydrochloride

NDC 33342-061 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202631
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (23 mg/1)
Marketing started20140123
Package count3

External sources

Source: openFDA. Public-domain (CC0).