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lacosamide

NDC 68462-679 · Glenmark Pharmaceuticals Inc. USA

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

68462-679-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (68462-679-10)

68462-679-30 — 30 TABLET, FILM COATED in 1 BOTTLE (68462-679-30)

68462-679-60 — 60 TABLET, FILM COATED in 1 BOTTLE (68462-679-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1445 — LACOSAMIDE, 67877-732 — Lacosamide Oral Solution, 67877-733 — Lacosamide, 67877-734 — Lacosamide, 67877-735 — Lacosamide, 67877-736 — Lacosamide, 68083-480 — Lacosamide, 68094-076 — LACOSAMIDE, 68094-176 — LACOSAMIDE, 68462-678 — lacosamide, 68462-680 — lacosamide, 68462-681 — lacosamide, 68462-697 — LACOSAMIDE, 68462-940 — Lacosamide, 68999-885 — Lacosamide, 69315-318 — Lacosamide, 69367-348 — Lacosamide, 69367-349 — Lacosamide, 69367-350 — Lacosamide, 69367-351 — 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.