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lamotrigine

NDC 31722-243 · Camber Pharmaceuticals Inc

Generic namelamotrigine extended-release
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
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

31722-243-30 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-243-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

27241-184 — Lamotrigine, 27241-185 — Lamotrigine, 27241-186 — Lamotrigine, 29300-111 — Lamotrigine, 29300-112 — Lamotrigine, 29300-113 — Lamotrigine, 29300-114 — Lamotrigine, 31722-240 — lamotrigine extended-release, 31722-241 — lamotrigine extended-release, 31722-242 — 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, 42291-444 — Lamotrigine, 42291-445 — Lamotrigine, 42291-446 — 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.