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Lamotrigine

NDC 70518-1978 · REMEDYREPACK INC.

Generic nameLamotrigine
Dosage formTABLET
RouteORAL
Active ingredient(s)LAMOTRIGINE
Strength150 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

70518-1978-0 — 30 TABLET in 1 BLISTER PACK (70518-1978-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69117-0047 — lamotrigine extended-release, 69117-0048 — lamotrigine extended-release, 69117-0049 — lamotrigine extended-release, 69918-350 — Lamotrigine, 69918-360 — Lamotrigine, 69918-370 — Lamotrigine, 69918-380 — Lamotrigine, 70518-1153 — Lamotrigine, 70518-1479 — Lamotrigine, 70518-1908 — 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, 70518-4638 — lamotrigine extended-release, +270 more

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