NDC 58118-8815 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC58118-8815

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Clinical Solutions Wholesale, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204787
Marketed since
March 17, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
58118-8815-830 TABLET, FILM COATED in 1 BLISTER PACK (58118-8815-8)Mar 24, 2026

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