NDC 46708-451 – Memantine Hydrochloride

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

Human Prescription Drug

Product NDC46708-451

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
46708-451-10100 TABLET, COATED in 1 CARTON (46708-451-10)Oct 13, 2015
46708-451-2020 TABLET, COATED in 1 BOTTLE (46708-451-20)Oct 13, 2015
46708-451-3030 TABLET, COATED in 1 BOTTLE (46708-451-30)Oct 13, 2015
46708-451-31100 TABLET, COATED in 1 BOTTLE (46708-451-31)Oct 13, 2015
46708-451-423000 TABLET, COATED in 1 BOTTLE (46708-451-42)Oct 13, 2015
46708-451-6060 TABLET, COATED in 1 BOTTLE (46708-451-60)Oct 13, 2015
46708-451-911000 TABLET, COATED in 1 BOTTLE (46708-451-91)Oct 13, 2015

Other Memantine hydrochloride products