United States · FDA National Drug Code directory
LAMICTAL
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
- 0173-0642_076c76e0-4a5e-491b-ba85-de2dd757b436
- Product NDC
- 0173-0642
- Form
- TABLET
- Composition / generic term
- lamotrigine
- Labeler
- GlaxoSmithKline LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 19950117
- Source listing expiry
- 20271231
Source-listed ingredients
- LAMOTRIGINE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0173-0642-55) · 0173-0642-55
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 →