memantine hydrochloride

FDA Drug Profile — memantine hydrochloride, Memantine Hydrochloride, MEMANTINE

memantine hydrochloride is listed in the FDA National Drug Code directory with 42 NDC codes, marketed under brand names including memantine hydrochloride, Memantine Hydrochloride, MEMANTINE. Available dosage forms: capsule, extended release, tablet, film coated, tablet, kit, tablet, coated.

Drug Details

Generic Name
memantine hydrochloride
Brand Names
memantine hydrochloride, Memantine Hydrochloride, MEMANTINE
Application Number
ANDA206028
Sponsor
Allergan, Inc.
NDC Codes
42
Dosage Forms
CAPSULE, EXTENDED RELEASE, TABLET, FILM COATED, TABLET, KIT, TABLET, COATED, SOLUTION
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 )