NDC 0832-1113 – Memantine Hydrochloride

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

Human Prescription Drug

Product NDC0832-1113

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine Hydrochloride
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090043
Marketed since
July 31, 2015
Marketing end
January 31, 2028
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
0832-1113-6060 TABLET, FILM COATED in 1 BOTTLE (0832-1113-60)Jul 31, 2015

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