NDC 60687-173 – Memantine

Memantine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-173

Product details

Brand name
Memantine
Generic name
Memantine
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090048
Marketed since
August 3, 2015
Listing expires
December 31, 2026
Pharmacologic class
N-methyl-D-aspartate Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Memantine →

Package NDC codes (1)

Package NDCDescriptionSince
60687-173-5760 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-173-57) / 1 TABLET in 1 BLISTER PACK (60687-173-11)Aug 3, 2015

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