NDC 69117-0047 – Lamotrigine

Lamotrigine 200 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC69117-0047

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine extended-release
Labeler
Yiling Pharmaceutical, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213949
Marketed since
December 9, 2021
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
69117-0047-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0047-1)Dec 9, 2021
69117-0047-2100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0047-2)Dec 9, 2021
69117-0047-3500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0047-3)Dec 9, 2021

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