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Donepezil hydrochloride

NDC 42799-954 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA203713
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (23 mg/1)
Marketing started20160219
Package count2

External sources

Source: openFDA. Public-domain (CC0).