FDA NDC Directory · JSON-LD · Markdown

Memantine hydrochloride

NDC 53746-173 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameMemantine
Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090041
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20150430
Package count3

External sources

Source: openFDA. Public-domain (CC0).