NDC 65162-988 – Lamotrigine

Lamotrigine 250 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65162-988

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207497
Marketed since
November 30, 2018
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 (2)

Package NDCDescriptionSince
65162-988-0330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-988-03)Nov 30, 2018
65162-988-0990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-988-09)Nov 30, 2018

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