NDC 71335-2328 – Lamotrigine

Lamotrigine 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2328

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077633
Marketed since
January 27, 2009
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lamotrigine →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2328-130 TABLET in 1 BOTTLE (71335-2328-1)Jan 9, 2024
71335-2328-260 TABLET in 1 BOTTLE (71335-2328-2)Jun 16, 2025
71335-2328-390 TABLET in 1 BOTTLE (71335-2328-3)Jan 2, 2024
71335-2328-4120 TABLET in 1 BOTTLE (71335-2328-4)Jun 16, 2025
71335-2328-545 TABLET in 1 BOTTLE (71335-2328-5)Jun 16, 2025
71335-2328-6180 TABLET in 1 BOTTLE (71335-2328-6)Jun 16, 2025
71335-2328-714 TABLET in 1 BOTTLE (71335-2328-7)Jun 16, 2025
71335-2328-8100 TABLET in 1 BOTTLE (71335-2328-8)May 9, 2024

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