NDC 29300-112 – Lamotrigine

Lamotrigine 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC29300-112

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090170
Marketed since
November 1, 2011
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 (3)

Package NDCDescriptionSince
29300-112-01100 TABLET in 1 BOTTLE, PLASTIC (29300-112-01)Nov 1, 2011
29300-112-05500 TABLET in 1 BOTTLE, PLASTIC (29300-112-05)Nov 1, 2011
29300-112-101000 TABLET in 1 BOTTLE, PLASTIC (29300-112-10)Nov 1, 2011

Recalls mentioning this NDC

Other Lamotrigine products