NDC 16571-855 – Memantine Hydrochloride

Memantine Hydrochloride 28 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC16571-855

Product details

Brand name
Memantine Hydrochloride
Generic name
Memantine
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206032
Marketed since
June 1, 2025
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 (2)

Package NDCDescriptionSince
16571-855-0330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-855-03)Jun 1, 2025
16571-855-0990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-855-09)Jun 1, 2025

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