NDC 46708-174 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC46708-174

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204974
Marketed since
March 18, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (4)

Package NDCDescriptionSince
46708-174-10100 TABLET, FILM COATED in 1 CARTON (46708-174-10)Mar 18, 2022
46708-174-3030 TABLET, FILM COATED in 1 BOTTLE (46708-174-30)Mar 18, 2022
46708-174-6060 TABLET, FILM COATED in 1 BOTTLE (46708-174-60)Mar 18, 2022
46708-174-71500 TABLET, FILM COATED in 1 BOTTLE (46708-174-71)Mar 18, 2022

Other Lacosamide products