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Memantine Hydrochloride

NDC 62332-075 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic namememantine hydrochloride
Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200891
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20151013
Package count7

External sources

Source: openFDA. Public-domain (CC0).