NDC 50228-195 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC50228-195

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
ScieGen Pharmaceuticals Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205237
Marketed since
March 18, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (3)

Package NDCDescriptionSince
50228-195-101000 TABLET, FILM COATED in 1 BOTTLE (50228-195-10)Mar 18, 2022
50228-195-3030 TABLET, FILM COATED in 1 BOTTLE (50228-195-30)Mar 18, 2022
50228-195-6060 TABLET, FILM COATED in 1 BOTTLE (50228-195-60)Mar 18, 2022

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