NDC 0173-0754 – Lamictal Xr

Lamotrigine 25 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0173-0754

Product details

Brand name
Lamictal Xr
Generic name
Lamotrigine
Labeler
GlaxoSmithKline LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
NDA · NDA022115
Marketed since
July 6, 2009
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lamictal →

Package NDC codes (1)

Package NDCDescriptionSince
0173-0754-0030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0754-00)Jul 6, 2009

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