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Memantine Hydrochloride

NDC 33342-297 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202840
Dosage form / routeTABLET · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20151013
Package count3

External sources

Source: openFDA. Public-domain (CC0).