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Lamotrigine

NDC 46708-277 · Alembic Pharmaceuticals Limited

Generic nameLamotrigine
Dosage formTABLET
RouteORAL
Active ingredient(s)LAMOTRIGINE
Strength200 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

46708-277-30 — 30 TABLET in 1 BOTTLE (46708-277-30)

46708-277-31 — 100 TABLET in 1 BOTTLE (46708-277-31)

46708-277-60 — 60 TABLET in 1 BOTTLE (46708-277-60)

46708-277-91 — 1000 TABLET in 1 BOTTLE (46708-277-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 46708-275 — Lamotrigine, 46708-276 — 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, 49884-485 — Lamotrigine, 49884-486 — 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.