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Memantine Hydrochloride

NDC 61442-192 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCarlsbad Technology, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212947
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (5 mg/1)
Marketing started20250622
Package count2

External sources

Source: openFDA. Public-domain (CC0).