Lamotrigine

NDC 50090-2131 · A-S Medication Solutions

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

50090-2131-0 — 60 TABLET in 1 BOTTLE (50090-2131-0)

50090-2131-1 — 30 TABLET in 1 BOTTLE (50090-2131-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 50090-2129 — Lamotrigine, 50090-2130 — Lamotrigine, 50090-3914 — Lamotrigine, 50090-5850 — Lamotrigine, 50090-6028 — LAMOTRIGINE, 50228-319 — Lamotrigine, 50228-320 — Lamotrigine, 50228-321 — Lamotrigine, 50228-322 — Lamotrigine, 51655-719 — Lamotrigine, 51655-855 — LAMOTRIGINE, 51672-4130 — 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.