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Lamotrigine

NDC 71335-0830 · Bryant Ranch Prepack

Generic nameLamotrigine
Dosage formTABLET
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

71335-0830-1 — 30 TABLET in 1 BOTTLE (71335-0830-1)

71335-0830-2 — 60 TABLET in 1 BOTTLE (71335-0830-2)

71335-0830-3 — 90 TABLET in 1 BOTTLE (71335-0830-3)

71335-0830-4 — 45 TABLET in 1 BOTTLE (71335-0830-4)

71335-0830-5 — 180 TABLET in 1 BOTTLE (71335-0830-5)

71335-0830-6 — 14 TABLET in 1 BOTTLE (71335-0830-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4638 — lamotrigine extended-release, 70518-4702 — Lamotrigine, 70771-1514 — Lamotirigine, 70771-1515 — Lamotirigine, 70771-1516 — Lamotirigine, 70771-1517 — Lamotirigine, 70771-1518 — Lamotirigine, 70771-1519 — Lamotirigine, 71205-245 — Lamotrigine, 71335-0706 — Lamotrigine, 71335-1110 — Lamotrigine, 71335-1179 — Lamotrigine, 71335-1469 — Lamotrigine, 71335-1919 — Lamotrigine, 71335-2071 — Lamotrigine, 71335-2328 — Lamotrigine, 71335-2384 — Lamotrigine, 72189-063 — LAMOTRIGINE, 72189-467 — Lamotrigine ER, 72189-560 — Lamotrigine ER, +270 more

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