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
- 82804-068_6f7e59d2-4311-42a0-93a0-b29b0417d96f
- Product NDC
- 82804-068
- Form
- TABLET
- Composition / generic term
- Lamotrigine
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111101
- Source listing expiry
- 20261231
Source-listed ingredients
- LAMOTRIGINE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (82804-068-30) · 82804-068-30
- 60 TABLET in 1 BOTTLE, PLASTIC (82804-068-60) · 82804-068-60
- 90 TABLET in 1 BOTTLE, PLASTIC (82804-068-90) · 82804-068-90
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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