Lamotrigine

NDC 42291-368 · AvKARE

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

42291-368-50 — 500 TABLET in 1 BOTTLE (42291-368-50)

42291-368-60 — 60 TABLET in 1 BOTTLE (42291-368-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29300-113 — Lamotrigine, 29300-114 — Lamotrigine, 31722-240 — lamotrigine extended-release, 31722-241 — lamotrigine extended-release, 31722-242 — lamotrigine extended-release, 31722-243 — lamotrigine extended-release, 31722-244 — lamotrigine extended-release, 31722-245 — lamotrigine extended-release, 42291-366 — Lamotrigine, 42291-367 — Lamotrigine, 42291-369 — Lamotrigine, 42291-443 — Lamotrigine, 42291-444 — Lamotrigine, 42291-445 — Lamotrigine, 42291-446 — Lamotrigine, 42291-447 — Lamotrigine, 42291-448 — Lamotrigine, 43063-203 — LAMOTRIGINE, 43063-238 — LAMOTRIGINE, 43598-550 — Lamotrigine, +270 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.