Lamotrigine

NDC 46708-275 · Alembic Pharmaceuticals Limited

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

46708-275-30 — 30 TABLET in 1 BOTTLE (46708-275-30)

46708-275-31 — 100 TABLET in 1 BOTTLE (46708-275-31)

46708-275-71 — 500 TABLET in 1 BOTTLE (46708-275-71)

46708-275-91 — 1000 TABLET in 1 BOTTLE (46708-275-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42291-448 — Lamotrigine, 43063-203 — LAMOTRIGINE, 43063-238 — LAMOTRIGINE, 43598-550 — Lamotrigine, 43598-551 — Lamotrigine, 43598-552 — Lamotrigine, 43598-553 — Lamotrigine, 46708-095 — lamotrigine chewable dispersible, 46708-096 — lamotrigine chewable dispersible, 46708-274 — Lamotrigine, 46708-276 — Lamotrigine, 46708-277 — Lamotrigine, 46708-417 — Lamotrigine, 46708-418 — Lamotrigine, 46708-419 — Lamotrigine, 46708-770 — Lamotrigine, 46708-771 — Lamotrigine, 46708-772 — Lamotrigine, 46708-773 — Lamotrigine, 49884-484 — 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.