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
- 72578-003_2dee57d8-27d7-481c-b1c9-21375e258a1b
- Product NDC
- 72578-003
- Form
- TABLET
- Composition / generic term
- Memantine Hydrochloride
- Labeler
- Viona Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190228
- 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 in 1 BOTTLE (72578-003-01) · 72578-003-01
- 500 TABLET in 1 BOTTLE (72578-003-05) · 72578-003-05
- 1000 TABLET in 1 BOTTLE (72578-003-10) · 72578-003-10
- 60 TABLET in 1 BOTTLE (72578-003-14) · 72578-003-14
- 10 BLISTER PACK in 1 CARTON (72578-003-77) / 10 TABLET in 1 BLISTER PACK (72578-003-30) · 72578-003-77
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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