NDC 49884-561 – Lamotrigine Extended Release

Lamotrigine 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC49884-561

Product details

Brand name
Lamotrigine Extended Release
Generic name
Lamotrigine extended release
Labeler
Par Health USA, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201791
Marketed since
January 18, 2013
Marketing end
September 30, 2026
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lamotrigine Extended Release →

Package NDC codes (1)

Package NDCDescriptionSince
49884-561-1130 TABLET in 1 BOTTLE (49884-561-11)Jan 18, 2013

Recalls mentioning this NDC

Other Lamotrigine Extended Release products