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Memantine Hydrochloride

NDC 65862-652 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203175
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20151013
Package count4

External sources

Source: openFDA. Public-domain (CC0).