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Donepezil Hydrochloride

NDC 42658-119 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205269
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (5 mg/1)
Marketing started20250101
Package count4

External sources

Source: openFDA. Public-domain (CC0).