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Memantine hydrochloride

NDC 52605-072 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPOLYGEN PHARMACEUTICALS INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA210587
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (10 mg/1)
Marketing started20210701
Package count3

External sources

Source: openFDA. Public-domain (CC0).