LACOSAMIDE

NDC 58118-8812 · Clinical Solutions Wholesale, LLC

Generic nameLACOSAMIDE

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LACOSAMIDE

Strength50 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

DEA scheduleCV

Marketing categoryANDA

Packages

58118-8812-8 — 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-8812-8)

FDA lists these products with the same active ingredient.

51407-723 — LACOSAMIDE, 51407-724 — LACOSAMIDE, 51991-348 — LACOSAMIDE, 51991-349 — LACOSAMIDE, 51991-350 — LACOSAMIDE, 51991-351 — LACOSAMIDE, 53746-923 — Lacosamide, 53746-924 — Lacosamide, 53746-925 — Lacosamide, 53746-926 — Lacosamide, 58118-8813 — LACOSAMIDE, 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, +141 more

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