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Memantine Hydrochloride

NDC 69680-162 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic namememantine hydrochloride
Labeler / ManufacturerVitruvias Therapeutics, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213985
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (14 mg/1)
Marketing started20231215
Package count1

External sources

Source: openFDA. Public-domain (CC0).