NDC 68382-982 – Lamotrigine

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

Human Prescription Drug

Product NDC68382-982

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207763
Marketed since
May 14, 2020
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
68382-982-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-982-05)May 14, 2020
68382-982-0630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-982-06)May 14, 2020
68382-982-1690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-982-16)May 14, 2020

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