NDC 53746-169 – Memantine hydrochloride

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

Human Prescription Drug

Product NDC53746-169

Product details

Brand name
Memantine hydrochloride
Generic name
Memantine
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090041
Marketed since
April 30, 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 (3)

Package NDCDescriptionSince
53746-169-101000 TABLET, FILM COATED in 1 BOTTLE (53746-169-10)Apr 30, 2015
53746-169-3030 TABLET, FILM COATED in 1 BOTTLE (53746-169-30)Apr 30, 2015
53746-169-6060 TABLET, FILM COATED in 1 BOTTLE (53746-169-60)Apr 30, 2015

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