Lacosamide

NDC 16714-548 · NorthStar RxLLC

Generic nameLacosamide

Dosage formTABLET

RouteORAL

Active ingredient(s)LACOSAMIDE

Strength50 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

DEA scheduleCV

Marketing categoryANDA

Packages

16714-548-01 — 60 TABLET in 1 BOTTLE (16714-548-01)

FDA lists these products with the same active ingredient.

10135-799 — Lacosamide, 10135-800 — Lacosamide, 10135-801 — Lacosamide, 10135-802 — Lacosamide, 13811-207 — Lacosamide, 14445-129 — Lacosamide, 14445-130 — Lacosamide, 14445-131 — Lacosamide, 14445-132 — Lacosamide, 14445-406 — Lacosamide, 16714-549 — Lacosamide, 16714-550 — Lacosamide, 16714-552 — Lacosamide, 25021-791 — LACOSAMIDE, 27808-243 — Lacosamide, 27808-244 — Lacosamide, 27808-245 — Lacosamide, 27808-246 — Lacosamide, 29300-364 — Lacosamide, 29300-365 — 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.