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: 68788-7871_2a1f59e0-2c69-4fa9-ab8a-1f7a2163aad7
Product NDC: 68788-7871
Form: TABLET
Composition / generic term: Lamotrigine
Labeler: Preferred Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20210215
Source listing expiry: 20271231

Source-listed ingredients

LAMOTRIGINE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (68788-7871-3) · 68788-7871-3
60 TABLET in 1 BOTTLE (68788-7871-6) · 68788-7871-6
90 TABLET in 1 BOTTLE (68788-7871-9) · 68788-7871-9

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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