NDC 55111-597 – Memantine Hydrochloride

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

Human Prescription Drug

Product NDC55111-597

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine Hydrochloride
Labeler
Dr. Reddys Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090048
Marketed since
July 11, 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 (6)

Package NDCDescriptionSince
55111-597-01100 TABLET, FILM COATED in 1 BOTTLE (55111-597-01)Jul 11, 2015
55111-597-05500 TABLET, FILM COATED in 1 BOTTLE (55111-597-05)Jul 11, 2015
55111-597-3030 TABLET, FILM COATED in 1 BOTTLE (55111-597-30)Jul 11, 2015
55111-597-6060 TABLET, FILM COATED in 1 BOTTLE (55111-597-60)Jul 11, 2015
55111-597-7810 BLISTER PACK in 1 CARTON (55111-597-78) / 10 TABLET, FILM COATED in 1 BLISTER PACKJul 11, 2015
55111-597-791 BLISTER PACK in 1 CARTON (55111-597-79) / 10 TABLET, FILM COATED in 1 BLISTER PACKJul 11, 2015

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