LACOSAMIDE

NDC 31722-813 · Camber Pharmaceuticals, Inc.

Generic nameLACOSAMIDE

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LACOSAMIDE

Strength100 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

DEA scheduleCV

Marketing categoryANDA

Packages

31722-813-05 — 500 TABLET, FILM COATED in 1 BOTTLE (31722-813-05)

31722-813-18 — 180 TABLET, FILM COATED in 1 BOTTLE (31722-813-18)

31722-813-32 — 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-813-32)

31722-813-60 — 60 TABLET, FILM COATED in 1 BOTTLE (31722-813-60)

FDA lists these products with the same active ingredient.

27808-244 — Lacosamide, 27808-245 — Lacosamide, 27808-246 — Lacosamide, 29300-364 — Lacosamide, 29300-365 — Lacosamide, 29300-366 — Lacosamide, 29300-367 — Lacosamide, 31722-203 — LACOSAMIDE, 31722-627 — Lacosamide, 31722-812 — LACOSAMIDE, 31722-814 — LACOSAMIDE, 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, +141 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.