Lacosamide

NDC 47335-918 · Sun Pharmaceutical Industries, 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

47335-918-18 — 1000 TABLET, FILM COATED in 1 BOTTLE (47335-918-18)

47335-918-82 — 180 TABLET, FILM COATED in 1 BOTTLE (47335-918-82)

47335-918-86 — 60 TABLET, FILM COATED in 1 BOTTLE (47335-918-86)

FDA lists these products with the same active ingredient.

31722-815 — LACOSAMIDE, 33342-302 — Lacosamide, 33342-303 — Lacosamide, 33342-304 — Lacosamide, 33342-305 — Lacosamide, 43598-087 — Lacosamide, 46708-171 — lacosamide, 46708-172 — lacosamide, 46708-173 — lacosamide, 46708-174 — lacosamide, 47335-922 — Lacosamide, 47335-943 — Lacosamide, 47335-980 — Lacosamide, 50228-192 — LACOSAMIDE, 50228-193 — LACOSAMIDE, 50228-194 — LACOSAMIDE, 50228-195 — LACOSAMIDE, 51407-721 — LACOSAMIDE, 51407-722 — LACOSAMIDE, 51407-723 — 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.