Lamotrigine

NDC 80425-0289 · Advanced Rx Pharmacy of Tennessee, LLC

Generic nameLamotrigine

Dosage formTABLET

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

80425-0289-1 — 30 TABLET in 1 BOTTLE (80425-0289-1)

80425-0289-2 — 60 TABLET in 1 BOTTLE (80425-0289-2)

80425-0289-3 — 90 TABLET in 1 BOTTLE (80425-0289-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 82009-131 — Lamotrigine, 82009-132 — Lamotrigine, 82009-133 — Lamotrigine, 82009-134 — Lamotrigine, 82804-022 — lamotrigine extended-release, 82804-068 — Lamotrigine, 82804-105 — Lamotrigine, 82868-005 — Lamotrigine, 84677-031 — lamotrigine, 84677-032 — 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.