NDC 47335-322 – Memantine Hydrochloride

Memantine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC47335-322

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090058
Marketed since
July 11, 2015
Listing expires
December 31, 2026
Pharmacologic class
N-methyl-D-aspartate Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for memantine hydrochloride →

Package NDC codes (6)

Package NDCDescriptionSince
47335-322-08100 TABLET, FILM COATED in 1 BOTTLE (47335-322-08)Jul 11, 2015
47335-322-13500 TABLET, FILM COATED in 1 BOTTLE (47335-322-13)Jul 11, 2015
47335-322-181000 TABLET, FILM COATED in 1 BOTTLE (47335-322-18)Jul 11, 2015
47335-322-8330 TABLET, FILM COATED in 1 BOTTLE (47335-322-83)Jul 11, 2015
47335-322-8660 TABLET, FILM COATED in 1 BOTTLE (47335-322-86)Jul 11, 2015
47335-322-88100 TABLET, FILM COATED in 1 BOTTLE (47335-322-88)Jul 11, 2015

Other memantine hydrochloride products