memantine

FDA Drug Profile — Memantine Hydrochloride, memantine, memantine hydrochloride

memantine is listed in the FDA National Drug Code directory with 8 NDC codes, marketed under brand names including Memantine Hydrochloride, memantine, memantine hydrochloride. Available dosage forms: capsule, extended release, tablet, tablet, film coated.

Drug Details

Generic Name
memantine
Brand Names
Memantine Hydrochloride, memantine, memantine hydrochloride
Application Number
ANDA206032
Sponsor
Rising Pharma Holdings, Inc.
NDC Codes
8
Dosage Forms
CAPSULE, EXTENDED RELEASE, TABLET, TABLET, FILM COATED
Routes
ORAL
Active Ingredients
MEMANTINE HYDROCHLORIDE

Indications and Usage

1 INDICATIONS AND USAGE Memantine hydrochloride oral solution is indicated for the treatment of moderate to severe dementia of the Alzheimer's type. Memantine hydrochloride oral solution is an N-methyl-D-aspartate (NMDA) receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer's type. ( 1 )