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Lamotrigine

NDC 55111-719 · Dr.Reddy's Laboratories Limited

Generic nameLamotrigine
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)LAMOTRIGINE
Strength100 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

55111-719-05 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-719-05)

55111-719-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-719-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55111-220 — Lamotrigine, 55111-221 — Lamotrigine, 55111-222 — Lamotrigine, 55111-223 — Lamotrigine, 55111-225 — Lamotrigine, 55111-226 — Lamotrigine, 55111-419 — Lamotrigine, 55111-428 — Lamotrigine, 55111-717 — Lamotrigine, 55111-718 — Lamotrigine, 55111-720 — Lamotrigine, 55154-2065 — Lamotrigine, 55154-2330 — Lamotrigine, 55154-2331 — Lamotrigine, 59746-245 — Lamotrigine, 59746-246 — Lamotrigine, 59746-247 — Lamotrigine, 59746-248 — Lamotrigine, 60687-693 — Lamotrigine, 60687-704 — 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.