NDC 50268-588 – Memantine Hydrochloride

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

Human Prescription Drug

Product NDC50268-588

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine hydrochloride
Labeler
AvPAK
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200022
Marketed since
February 20, 2024
Listing expires
December 31, 2027
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
50268-588-1330 BLISTER PACK in 1 BOX (50268-588-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-588-11)Feb 20, 2024

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