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
- 65162-949_cfe3f042-c606-4e0a-87d9-c306eab17230
- Product NDC
- 65162-949
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Lamotrigine
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181130
- Source listing expiry
- 20271231
Source-listed ingredients
- LAMOTRIGINE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-949-03) · 65162-949-03
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-949-09) · 65162-949-09
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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