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Lacosamide

NDC 47335-943 · Sun Pharmaceutical Industries, Inc.

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

47335-943-18 — 1000 TABLET, FILM COATED in 1 BOTTLE (47335-943-18)

47335-943-82 — 180 TABLET, FILM COATED in 1 BOTTLE (47335-943-82)

47335-943-86 — 60 TABLET, FILM COATED in 1 BOTTLE (47335-943-86)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-303 — Lacosamide, 33342-304 — Lacosamide, 33342-305 — Lacosamide, 43598-087 — Lacosamide, 46708-171 — lacosamide, 46708-172 — lacosamide, 46708-173 — lacosamide, 46708-174 — lacosamide, 47335-918 — Lacosamide, 47335-922 — 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, 51407-724 — LACOSAMIDE, 51991-348 — 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.