Lamotrigine 51672-4255-06

Package NDC

51672-4255-06

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 27, 2026
Listing Expires: December 31, 2027
Application: ANDA219677

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Active Ingredients

Ingredient	Strength
Lamotrigine	200 mg/1

Drug Class

Anti-epileptic Agent [EPC]Mood Stabilizer [EPC]Anti-epileptic Agent [EPC]

Selected Package

51672-4255-06Selected

30 TABLET in 1 BOTTLE (51672-4255-6)