United States · FDA National Drug Code directory
lacosamide
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
- 68462-678_a496c733-ce38-4566-83f9-0287506f4506
- Product NDC
- 68462-678
- Form
- TABLET, FILM COATED
- Composition / generic term
- lacosamide
- Labeler
- Glenmark Pharmaceuticals Inc. USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220318
- Source listing expiry
- 20261231
Source-listed ingredients
- LACOSAMIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (68462-678-10) · 68462-678-10
- 30 TABLET, FILM COATED in 1 BOTTLE (68462-678-30) · 68462-678-30
- 60 TABLET, FILM COATED in 1 BOTTLE (68462-678-60) · 68462-678-60
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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