Lacosamide

NDC 71921-220 · Florida Pharmaceutical Products, LLC

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

71921-220-06 — 60 TABLET in 1 BOTTLE (71921-220-06)

FDA lists these products with the same active ingredient.

70518-4503 — lacosamide, 70518-4504 — lacosamide, 70518-4505 — lacosamide, 70518-4561 — Lacosamide, 70518-4562 — Lacosamide, 70518-4689 — Lacosamide, 70710-1359 — Lacosamide, 70710-1886 — Lacosamide, 70771-1682 — Lacosamide, 70954-488 — Lacosamide, 71921-221 — Lacosamide, 71921-222 — Lacosamide, 71921-223 — Lacosamide, 71921-411 — Lacosamide Oral, 72162-2637 — Lacosamide, 72205-034 — Lacosamide, 72205-220 — Lacosamide, 72266-242 — Lacosamide, 72603-263 — LACOSAMIDE, 72603-305 — 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.