United States · FDA National Drug Code directory
lamotrigine
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
- 69117-0048_47239426-3d75-73d8-e063-6294a90a608d
- Product NDC
- 69117-0048
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- lamotrigine extended-release
- Labeler
- Yiling Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211209
- Source listing expiry
- 20261231
Source-listed ingredients
- LAMOTRIGINE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0048-1) · 69117-0048-1
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0048-2) · 69117-0048-2
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0048-3) · 69117-0048-3
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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