NDC 65162-784 – Memantine Hydrochloride

Memantine Hydrochloride 21 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC65162-784

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205825
Marketed since
December 22, 2017
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 (3)

Package NDCDescriptionSince
65162-784-0330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-784-03)Dec 22, 2017
65162-784-0990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-784-09)Dec 22, 2017
65162-784-50500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-784-50)Dec 22, 2017

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