NDC 65162-173 – Memantine hydrochloride

Memantine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65162-173

Product details

Brand name
Memantine hydrochloride
Generic name
Memantine
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090041
Marketed since
March 24, 2022
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 (1)

Package NDCDescriptionSince
65162-173-0660 TABLET, FILM COATED in 1 BOTTLE (65162-173-06)Mar 24, 2022

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