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Lamotrigine

NDC 62332-038 · Alembic Pharmaceuticals 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

62332-038-30 — 30 TABLET in 1 BOTTLE (62332-038-30)

62332-038-31 — 100 TABLET in 1 BOTTLE (62332-038-31)

62332-038-71 — 500 TABLET in 1 BOTTLE (62332-038-71)

62332-038-91 — 1000 TABLET in 1 BOTTLE (62332-038-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-2065 — Lamotrigine, 55154-2330 — Lamotrigine, 55154-2331 — Lamotrigine, 59746-245 — Lamotrigine, 59746-246 — Lamotrigine, 59746-247 — Lamotrigine, 59746-248 — Lamotrigine, 60687-693 — Lamotrigine, 60687-704 — Lamotrigine, 62332-037 — Lamotrigine, 62332-039 — Lamotrigine, 62332-040 — Lamotrigine, 62332-095 — lamotrigine, 62332-096 — lamotrigine, 62332-417 — Lamotrigine, 62332-418 — Lamotrigine, 62332-419 — Lamotrigine, 62332-770 — Lamotrigine, 62332-771 — Lamotrigine, 62332-772 — 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.