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memantine hydrochloride and donepezil hydrochloride

NDC 69680-183 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerVitruvias Therapeutics, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216901
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDONEPEZIL HYDROCHLORIDE (10 mg/1)
MEMANTINE HYDROCHLORIDE (14 mg/1)
Marketing started20250716
Package count1

External sources

Source: openFDA. Public-domain (CC0).