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
- 71335-2384_2cf33586-e48a-4b4e-b14b-33de2be63c1d
- Product NDC
- 71335-2384
- Form
- TABLET
- Composition / generic term
- Lamotrigine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090127
- Source listing expiry
- 20261231
Source-listed ingredients
- LAMOTRIGINE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2384-1) · 71335-2384-1
- 60 TABLET in 1 BOTTLE (71335-2384-2) · 71335-2384-2
- 90 TABLET in 1 BOTTLE (71335-2384-3) · 71335-2384-3
- 100 TABLET in 1 BOTTLE (71335-2384-4) · 71335-2384-4
- 120 TABLET in 1 BOTTLE (71335-2384-5) · 71335-2384-5
- 14 TABLET in 1 BOTTLE (71335-2384-6) · 71335-2384-6
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 →