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Lamotrigine

NDC 55111-220 · Dr.Reddy's Laboratories Limited

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

55111-220-01 — 100 TABLET in 1 BOTTLE (55111-220-01)

55111-220-05 — 500 TABLET in 1 BOTTLE (55111-220-05)

55111-220-30 — 30 TABLET in 1 BOTTLE (55111-220-30)

55111-220-60 — 60 TABLET in 1 BOTTLE (55111-220-60)

55111-220-78 — 10 BLISTER PACK in 1 CARTON (55111-220-78) / 10 TABLET in 1 BLISTER PACK (55111-220-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-719 — Lamotrigine, 51655-855 — LAMOTRIGINE, 51672-4130 — Lamotrigine, 51672-4131 — Lamotrigine, 51672-4132 — Lamotrigine, 51672-4133 — Lamotrigine, 51672-4252 — lamotrigine, 51672-4253 — lamotrigine, 51672-4254 — lamotrigine, 51672-4255 — 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, 55111-719 — 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.