NDC 72578-003 – Memantine Hydrochloride

Memantine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72578-003

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine Hydrochloride
Labeler
Viona Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090961
Marketed since
February 28, 2019
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 (5)

Package NDCDescriptionSince
72578-003-01100 TABLET in 1 BOTTLE (72578-003-01)Feb 28, 2019
72578-003-05500 TABLET in 1 BOTTLE (72578-003-05)Feb 28, 2019
72578-003-101000 TABLET in 1 BOTTLE (72578-003-10)Feb 28, 2019
72578-003-1460 TABLET in 1 BOTTLE (72578-003-14)Feb 28, 2019
72578-003-7710 BLISTER PACK in 1 CARTON (72578-003-77) / 10 TABLET in 1 BLISTER PACK (72578-003-30)Feb 28, 2019

Other Memantine hydrochloride products