NDC 61442-192 – Memantine Hydrochloride

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

Human Prescription Drug

Product NDC61442-192

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine Hydrochloride
Labeler
Carlsbad Technology, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212947
Marketed since
June 22, 2025
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 (2)

Package NDCDescriptionSince
61442-192-05500 TABLET, FILM COATED in 1 BOTTLE (61442-192-05)Jun 22, 2025
61442-192-6060 TABLET, FILM COATED in 1 BOTTLE (61442-192-60)Jun 22, 2025

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