NDC 51672-4131 – Lamotrigine

Lamotrigine 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC51672-4131

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Sun Pharmaceutical Industries, Inc.
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
51672-4131-010 BLISTER PACK in 1 CARTON (51672-4131-0) / 10 TABLET in 1 BLISTER PACKJan 27, 2009
51672-4131-1100 TABLET in 1 BOTTLE (51672-4131-1)Jan 27, 2009
51672-4131-31000 TABLET in 1 BOTTLE (51672-4131-3)Jan 27, 2009
51672-4131-460 TABLET in 1 BOTTLE (51672-4131-4)Jan 27, 2009
51672-4131-630 TABLET in 1 BOTTLE (51672-4131-6)Jan 27, 2009

Recalls mentioning this NDC

Other Lamotrigine products