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Memantine Hydrochloride

NDC 70518-3338 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA090961
Dosage form / routeTABLET · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20220120
Package count1

External sources

Source: openFDA. Public-domain (CC0).