Lacosamide

NDC 70518-4689 · REMEDYREPACK INC.

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

70518-4689-0 — 30 POUCH in 1 BOX (70518-4689-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)

70518-4689-2 — 100 POUCH in 1 BOX (70518-4689-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)

FDA lists these products with the same active ingredient.

69539-026 — lacosamide, 69539-027 — lacosamide, 69539-028 — lacosamide, 69543-455 — LACOSAMIDE, 70069-471 — LACOSAMIDE, 70518-4503 — lacosamide, 70518-4504 — lacosamide, 70518-4505 — lacosamide, 70518-4561 — Lacosamide, 70518-4562 — Lacosamide, 70710-1359 — Lacosamide, 70710-1886 — Lacosamide, 70771-1682 — Lacosamide, 70954-488 — Lacosamide, 71921-220 — Lacosamide, 71921-221 — Lacosamide, 71921-222 — Lacosamide, 71921-223 — Lacosamide, 71921-411 — Lacosamide Oral, 72162-2637 — 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.