NDC 10135-799 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC10135-799

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Marlex Pharmaceuticals, Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA218014
Marketed since
May 23, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (2)

Package NDCDescriptionSince
10135-799-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-799-60)Jul 1, 2025
10135-799-866 BLISTER PACK in 1 CARTON (10135-799-86) / 10 TABLET, FILM COATED in 1 BLISTER PACKJul 1, 2025

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