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memantine hydrochloride

NDC 65162-169 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namememantine
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090041
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (10 mg/1)
Marketing started20220324
Package count1

External sources

Source: openFDA. Public-domain (CC0).