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Memantine Hydrochloride

NDC 70771-1119 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090961
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20170928
Package count5

External sources

Source: openFDA. Public-domain (CC0).