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
- 65162-782_fb7782a5-2357-4a21-86a6-0eeaa7cdcea5
- Product NDC
- 65162-782
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Memantine Hydrochloride
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171222
- Source listing expiry
- 20261231
Source-listed ingredients
- MEMANTINE HYDROCHLORIDE — 7 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-782-03) · 65162-782-03
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-782-09) · 65162-782-09
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-782-50) · 65162-782-50
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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