NDC 51672-4254 – Lamotrigine

Lamotrigine 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51672-4254

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA219677
Marketed since
March 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lamotrigine →

Package NDC codes (1)

Package NDCDescriptionSince
51672-4254-630 TABLET in 1 BOTTLE (51672-4254-6)Mar 1, 2026

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