NDC 59746-247 – Lamotrigine

Lamotrigine 150 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC59746-247

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Jubilant Cadista Pharmacuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079132
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 (3)

Package NDCDescriptionSince
59746-247-05500 TABLET in 1 BOTTLE (59746-247-05)Jan 27, 2009
59746-247-6060 TABLET in 1 BOTTLE (59746-247-60)Jan 27, 2009
59746-247-9090 TABLET in 1 BOTTLE (59746-247-90)Jan 27, 2009

Recalls mentioning this NDC

Other Lamotrigine products