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
- 55111-597_998c5d15-8b47-fe20-82c5-98897caf80eb
- Product NDC
- 55111-597
- Form
- TABLET, FILM COATED
- Composition / generic term
- Memantine Hydrochloride
- Labeler
- Dr. Reddys Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150711
- Source listing expiry
- 20261231
Source-listed ingredients
- MEMANTINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (55111-597-01) · 55111-597-01
- 500 TABLET, FILM COATED in 1 BOTTLE (55111-597-05) · 55111-597-05
- 30 TABLET, FILM COATED in 1 BOTTLE (55111-597-30) · 55111-597-30
- 60 TABLET, FILM COATED in 1 BOTTLE (55111-597-60) · 55111-597-60
- 10 BLISTER PACK in 1 CARTON (55111-597-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 55111-597-78
- 1 BLISTER PACK in 1 CARTON (55111-597-79) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 55111-597-79
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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