NDC 71335-0830 – Lamotrigine

Lamotrigine 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0830

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090170
Marketed since
November 1, 2011
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 (6)

Package NDCDescriptionSince
71335-0830-130 TABLET in 1 BOTTLE (71335-0830-1)Feb 9, 2022
71335-0830-260 TABLET in 1 BOTTLE (71335-0830-2)Feb 9, 2022
71335-0830-390 TABLET in 1 BOTTLE (71335-0830-3)Feb 9, 2022
71335-0830-445 TABLET in 1 BOTTLE (71335-0830-4)Feb 9, 2022
71335-0830-5180 TABLET in 1 BOTTLE (71335-0830-5)Feb 9, 2022
71335-0830-614 TABLET in 1 BOTTLE (71335-0830-6)Feb 9, 2022

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