NDC 70518-4504 – Lacosamide

Lacosamide 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV

Product NDC70518-4504

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204974
Marketed since
October 14, 2025
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (3)

Package NDCDescriptionSince
70518-4504-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4504-0)Oct 14, 2025
70518-4504-130 POUCH in 1 BOX (70518-4504-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4504-2)Feb 2, 2026
70518-4504-350 POUCH in 1 BOX (70518-4504-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-4504-2)Jul 20, 2026

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