FDA NDC Directory · JSON-LD · Markdown

donepezil hydrochloride

NDC 29300-250 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204831
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (5 mg/1)
Marketing started20161110
Package count1

External sources

Source: openFDA. Public-domain (CC0).