Lamotrigine

NDC 71335-2328 · Bryant Ranch Prepack

Generic nameLamotrigine

Dosage formTABLET

RouteORAL

Active ingredient(s)LAMOTRIGINE

Strength100 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

71335-2328-1 30 TABLET in 1 BOTTLE (71335-2328-1)

71335-2328-2 60 TABLET in 1 BOTTLE (71335-2328-2)

71335-2328-3 90 TABLET in 1 BOTTLE (71335-2328-3)

71335-2328-4 120 TABLET in 1 BOTTLE (71335-2328-4)

71335-2328-5 45 TABLET in 1 BOTTLE (71335-2328-5)

71335-2328-6 180 TABLET in 1 BOTTLE (71335-2328-6)

71335-2328-7 14 TABLET in 1 BOTTLE (71335-2328-7)

71335-2328-8 100 TABLET in 1 BOTTLE (71335-2328-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70771-1518 — Lamotirigine, 70771-1519 — Lamotirigine, 71205-245 — Lamotrigine, 71335-0706 — Lamotrigine, 71335-0830 — Lamotrigine, 71335-1110 — Lamotrigine, 71335-1179 — Lamotrigine, 71335-1469 — Lamotrigine, 71335-1919 — Lamotrigine, 71335-2071 — Lamotrigine, 71335-2384 — Lamotrigine, 72189-063 — LAMOTRIGINE, 72189-467 — Lamotrigine ER, 72189-560 — Lamotrigine ER, 72789-206 — Lamotrigine, 72888-025 — Lamotrigine, 72888-026 — Lamotrigine, 72888-027 — Lamotrigine, 72888-028 — Lamotrigine, 76420-182 — 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.