lamotrigine

NDC 70518-4638 · REMEDYREPACK INC.

Generic namelamotrigine extended-release

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)LAMOTRIGINE

Strength200 mg/1

Pharmacologic classAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA]

Marketing categoryANDA

Packages

70518-4638-0 — 50 POUCH in 1 BOX (70518-4638-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-4638-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-1978 — Lamotrigine, 70518-2343 — Lamotrigine, 70518-2406 — Lamotrigine, 70518-2563 — Lamotrigine, 70518-2577 — Lamotrigine, 70518-2755 — LAMOTRIGINE, 70518-2889 — LAMOTRIGINE, 70518-3043 — Lamotrigine, 70518-4121 — Lamotrigine, 70518-4442 — lamotrigine extended-release, 70518-4702 — Lamotrigine, 70771-1514 — Lamotirigine, 70771-1515 — Lamotirigine, 70771-1516 — Lamotirigine, 70771-1517 — Lamotirigine, 70771-1518 — Lamotirigine, 70771-1519 — Lamotirigine, 71205-245 — Lamotrigine, 71335-0706 — Lamotrigine, 71335-0830 — Lamotrigine, +270 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.