Lamotrigine

NDC 42291-444 · AvKARE

Generic nameLamotrigine

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)LAMOTRIGINE

Strength50 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

42291-444-30 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-444-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 42291-368 — Lamotrigine, 42291-369 — Lamotrigine, 42291-443 — Lamotrigine, 42291-445 — Lamotrigine, 42291-446 — Lamotrigine, 42291-447 — Lamotrigine, 42291-448 — Lamotrigine, 43063-203 — LAMOTRIGINE, 43063-238 — LAMOTRIGINE, 43598-550 — Lamotrigine, 43598-551 — Lamotrigine, 43598-552 — Lamotrigine, 43598-553 — 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.