NDC 71335-2071 – Lamotrigine

Lamotrigine 150 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2071

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078525
Marketed since
January 27, 2009
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 (5)

Package NDCDescriptionSince
71335-2071-160 TABLET in 1 BOTTLE (71335-2071-1)Apr 3, 2024
71335-2071-230 TABLET in 1 BOTTLE (71335-2071-2)Mar 25, 2022
71335-2071-390 TABLET in 1 BOTTLE (71335-2071-3)Apr 3, 2024
71335-2071-4120 TABLET in 1 BOTTLE (71335-2071-4)Apr 3, 2024
71335-2071-5180 TABLET in 1 BOTTLE (71335-2071-5)Apr 3, 2024

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