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
- 46708-452_3d66d5be-d570-4041-82bf-6b6f4eef9ed8
- Product NDC
- 46708-452
- Form
- TABLET, COATED
- Composition / generic term
- memantine hydrochloride
- Labeler
- Alembic 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
- 100 TABLET, COATED in 1 CARTON (46708-452-10) · 46708-452-10
- 20 TABLET, COATED in 1 BOTTLE (46708-452-20) · 46708-452-20
- 30 TABLET, COATED in 1 BOTTLE (46708-452-30) · 46708-452-30
- 100 TABLET, COATED in 1 BOTTLE (46708-452-31) · 46708-452-31
- 3000 TABLET, COATED in 1 BOTTLE (46708-452-42) · 46708-452-42
- 60 TABLET, COATED in 1 BOTTLE (46708-452-60) · 46708-452-60
- 500 TABLET, COATED in 1 BOTTLE (46708-452-71) · 46708-452-71
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →