NDC 46708-452 – Memantine Hydrochloride

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

Human Prescription Drug

Product NDC46708-452

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine hydrochloride
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA200891
Marketed since
October 13, 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 (7)

Package NDCDescriptionSince
46708-452-10100 TABLET, COATED in 1 CARTON (46708-452-10)Oct 13, 2015
46708-452-2020 TABLET, COATED in 1 BOTTLE (46708-452-20)Oct 13, 2015
46708-452-3030 TABLET, COATED in 1 BOTTLE (46708-452-30)Oct 13, 2015
46708-452-31100 TABLET, COATED in 1 BOTTLE (46708-452-31)Oct 13, 2015
46708-452-423000 TABLET, COATED in 1 BOTTLE (46708-452-42)Oct 13, 2015
46708-452-6060 TABLET, COATED in 1 BOTTLE (46708-452-60)Oct 13, 2015
46708-452-71500 TABLET, COATED in 1 BOTTLE (46708-452-71)Oct 13, 2015

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