LAMOTRIGINE
NDC 51672-4254 · Sun Pharmaceutical Industries, Inc.
Generic namelamotrigine
Dosage formTABLET
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
51672-4254-6 — 30 TABLET in 1 BOTTLE (51672-4254-6)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
50228-321 — Lamotrigine, 50228-322 — Lamotrigine, 51655-719 — Lamotrigine, 51655-855 — LAMOTRIGINE, 51672-4130 — Lamotrigine, 51672-4131 — Lamotrigine, 51672-4132 — Lamotrigine, 51672-4133 — Lamotrigine, 51672-4252 — lamotrigine, 51672-4253 — lamotrigine, 51672-4255 — lamotrigine, 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, +270 more