NDC 80425-0510 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC80425-0510

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214695
Marketed since
April 9, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0510-130 TABLET, FILM COATED in 1 BOTTLE (80425-0510-1)Apr 9, 2025
80425-0510-260 TABLET, FILM COATED in 1 BOTTLE (80425-0510-2)Apr 9, 2025
80425-0510-390 TABLET, FILM COATED in 1 BOTTLE (80425-0510-3)Apr 9, 2025

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