Lacosamide

NDC 62332-172 · Alembic Pharmaceuticals Inc.

Generic namelacosamide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LACOSAMIDE

Strength100 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

DEA scheduleCV

Marketing categoryANDA

Packages

62332-172-10 — 100 BLISTER PACK in 1 CARTON (62332-172-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

62332-172-30 — 30 TABLET, FILM COATED in 1 BOTTLE (62332-172-30)

62332-172-60 — 60 TABLET, FILM COATED in 1 BOTTLE (62332-172-60)

62332-172-91 — 1000 TABLET, FILM COATED in 1 BOTTLE (62332-172-91)

FDA lists these products with the same active ingredient.

58118-8814 — LACOSAMIDE, 58118-8815 — LACOSAMIDE, 59651-016 — Lacosamide, 60505-6235 — lacosamide, 60687-676 — Lacosamide, 60687-687 — Lacosamide, 60687-698 — Lacosamide, 60687-847 — Lacosamide, 62135-885 — Lacosamide, 62332-171 — lacosamide, 62332-173 — lacosamide, 62332-174 — lacosamide, 65219-204 — Lacosamide, 65862-747 — Lacosamide, 65862-748 — Lacosamide, 65862-749 — Lacosamide, 65862-750 — Lacosamide, 67046-1445 — LACOSAMIDE, 67877-732 — Lacosamide Oral Solution, 67877-733 — Lacosamide, +141 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.