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
- 47335-321_81ca8cbf-7854-43a2-bd0b-1dbaf4709a42
- Product NDC
- 47335-321
- Form
- TABLET, FILM COATED
- Composition / generic term
- Memantine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150711
- Source listing expiry
- 20261231
Source-listed ingredients
- MEMANTINE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (47335-321-08) · 47335-321-08
- 1000 TABLET, FILM COATED in 1 BOTTLE (47335-321-18) · 47335-321-18
- 60 TABLET, FILM COATED in 1 BOTTLE (47335-321-86) · 47335-321-86
- 100 TABLET, FILM COATED in 1 BOTTLE (47335-321-88) · 47335-321-88
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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