NDC 70518-4689 – Lacosamide

Lacosamide 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV

Product NDC70518-4689

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214695
Marketed since
July 3, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (3)

Package NDCDescriptionSince
70518-4689-030 POUCH in 1 BOX (70518-4689-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)Jul 3, 2026
70518-4689-2100 POUCH in 1 BOX (70518-4689-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)Jul 6, 2026
70518-4689-350 POUCH in 1 BOX (70518-4689-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)Sep 23, 2026

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