Lamotrigine

NDC 27241-186 · Ajanta Pharma USA Inc.

Generic nameLamotrigine

Dosage formTABLET, ORALLY DISINTEGRATING

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

27241-186-30 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (27241-186-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-197 — Lamotrigine, 16714-623 — Lamotrigine, 16714-624 — Lamotrigine, 16714-625 — Lamotrigine, 16714-626 — Lamotrigine, 16714-627 — Lamotrigine, 16714-893 — Lamotrigine, 27241-183 — Lamotrigine, 27241-184 — Lamotrigine, 27241-185 — Lamotrigine, 29300-111 — Lamotrigine, 29300-112 — Lamotrigine, 29300-113 — Lamotrigine, 29300-114 — Lamotrigine, 31722-240 — lamotrigine extended-release, 31722-241 — lamotrigine extended-release, 31722-242 — lamotrigine extended-release, 31722-243 — lamotrigine extended-release, 31722-244 — lamotrigine extended-release, 31722-245 — lamotrigine extended-release, +270 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.