Lacosamide

NDC 10135-802 · Marlex Pharmaceuticals, Inc

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

10135-802-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-802-60)

FDA lists these products with the same active ingredient.

0131-5410 — lacosamide, 0904-7244 — Lacosamide, 0904-7245 — Lacosamide, 0904-7246 — Lacosamide, 0904-7247 — Lacosamide, 0904-7463 — Lacosamide, 0904-7464 — Lacosamide, 10135-799 — Lacosamide, 10135-800 — Lacosamide, 10135-801 — Lacosamide, 13811-207 — Lacosamide, 14445-129 — Lacosamide, 14445-130 — Lacosamide, 14445-131 — Lacosamide, 14445-132 — Lacosamide, 14445-406 — Lacosamide, 16714-548 — Lacosamide, 16714-549 — Lacosamide, 16714-550 — Lacosamide, 16714-552 — 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.