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Memantine Hydrochloride

NDC 16571-855 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic namememantine
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206032
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (28 mg/1)
Marketing started20250601
Package count2

External sources

Source: openFDA. Public-domain (CC0).