United States · FDA National Drug Code directory

memantine hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 0591-3870_985e1190-b8a0-4775-9a20-ad1924b14fb2
Product NDC: 0591-3870
Form: TABLET
Composition / generic term: memantine hydrochloride
Labeler: Actavis Pharma, Inc.
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20150401 / 20280731

Source-listed ingredients

MEMANTINE HYDROCHLORIDE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

10 BLISTER PACK in 1 BOX, UNIT-DOSE (0591-3870-44) / 10 TABLET in 1 BLISTER PACK (0591-3870-45) · 0591-3870-44
60 TABLET in 1 BOTTLE (0591-3870-60) · 0591-3870-60

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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