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Lamotrigine

NDC 51672-4132 · Sun Pharmaceutical Industries, Inc.

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

51672-4132-0 — 10 BLISTER PACK in 1 CARTON (51672-4132-0) / 10 TABLET in 1 BLISTER PACK

51672-4132-1 — 100 TABLET in 1 BOTTLE (51672-4132-1)

51672-4132-3 — 1000 TABLET in 1 BOTTLE (51672-4132-3)

51672-4132-4 — 60 TABLET in 1 BOTTLE (51672-4132-4)

51672-4132-6 — 30 TABLET in 1 BOTTLE (51672-4132-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-5850 — Lamotrigine, 50090-6028 — LAMOTRIGINE, 50228-319 — Lamotrigine, 50228-320 — Lamotrigine, 50228-321 — Lamotrigine, 50228-322 — Lamotrigine, 51655-719 — Lamotrigine, 51655-855 — LAMOTRIGINE, 51672-4130 — Lamotrigine, 51672-4131 — Lamotrigine, 51672-4133 — Lamotrigine, 51672-4252 — lamotrigine, 51672-4253 — lamotrigine, 51672-4254 — lamotrigine, 51672-4255 — lamotrigine, 55111-220 — Lamotrigine, 55111-221 — Lamotrigine, 55111-222 — Lamotrigine, 55111-223 — Lamotrigine, 55111-225 — 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.