Lacosamide

NDC 60687-698 · American Health Packaging

Generic nameLacosamide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LACOSAMIDE

Strength200 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

DEA scheduleCV

Marketing categoryANDA

Packages

60687-698-57 — 60 BLISTER PACK in 1 CARTON (60687-698-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-698-11)

FDA lists these products with the same active ingredient.

53746-925 — Lacosamide, 53746-926 — Lacosamide, 58118-8812 — LACOSAMIDE, 58118-8813 — LACOSAMIDE, 58118-8814 — LACOSAMIDE, 58118-8815 — LACOSAMIDE, 59651-016 — Lacosamide, 60505-6235 — lacosamide, 60687-676 — Lacosamide, 60687-687 — Lacosamide, 60687-847 — Lacosamide, 62135-885 — Lacosamide, 62332-171 — lacosamide, 62332-172 — lacosamide, 62332-173 — lacosamide, 62332-174 — lacosamide, 65219-204 — Lacosamide, 65862-747 — Lacosamide, 65862-748 — Lacosamide, 65862-749 — 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.