Lamotrigine

NDC 46708-770 · Alembic Pharmaceuticals Limited

Generic nameLamotrigine

Dosage formTABLET, ORALLY DISINTEGRATING

RouteORAL

Active ingredient(s)LAMOTRIGINE

Strength25 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

46708-770-15 — 2 BLISTER PACK in 1 CARTON (46708-770-15) / 15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

46708-770-30 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (46708-770-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-553 — Lamotrigine, 46708-095 — lamotrigine chewable dispersible, 46708-096 — lamotrigine chewable dispersible, 46708-274 — Lamotrigine, 46708-275 — Lamotrigine, 46708-276 — Lamotrigine, 46708-277 — Lamotrigine, 46708-417 — Lamotrigine, 46708-418 — Lamotrigine, 46708-419 — Lamotrigine, 46708-771 — Lamotrigine, 46708-772 — Lamotrigine, 46708-773 — Lamotrigine, 49884-484 — Lamotrigine, 49884-485 — Lamotrigine, 49884-486 — Lamotrigine, 49884-487 — Lamotrigine, 49884-561 — lamotrigine extended release, 49884-604 — lamotrigine extended release, 49884-605 — 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.