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: 33342-298_672222e3-12b9-488f-a5ee-c47736d65cce
Product NDC: 33342-298
Form: TABLET
Composition / generic term: Memantine Hydrochloride
Labeler: Macleods Pharmaceuticals Limited
Marketing category: ANDA
Marketing start / end (source format): 20151013
Source listing expiry: 20261231

Source-listed ingredients

MEMANTINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

60 TABLET in 1 BOTTLE (33342-298-09) · 33342-298-09
10 BLISTER PACK in 1 CARTON (33342-298-12) / 10 TABLET in 1 BLISTER PACK · 33342-298-12
500 TABLET in 1 BOTTLE (33342-298-15) · 33342-298-15

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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