Lacosamide

NDC 69367-350 · Westminster Pharmaceuticals, LLC

Generic nameLacosamide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LACOSAMIDE

Strength150 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

DEA scheduleCV

Marketing categoryANDA

Packages

69367-350-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-350-60)

FDA lists these products with the same active ingredient.

68462-678 — lacosamide, 68462-679 — lacosamide, 68462-680 — lacosamide, 68462-681 — lacosamide, 68462-697 — LACOSAMIDE, 68462-940 — Lacosamide, 68999-885 — Lacosamide, 69315-318 — Lacosamide, 69367-348 — Lacosamide, 69367-349 — Lacosamide, 69367-351 — Lacosamide, 69367-352 — Lacosamide, 69539-025 — lacosamide, 69539-026 — lacosamide, 69539-027 — lacosamide, 69539-028 — lacosamide, 69543-455 — LACOSAMIDE, 70069-471 — LACOSAMIDE, 70518-4503 — lacosamide, 70518-4504 — 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.