NDC 68462-680 – Lacosamide

Lacosamide 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV 4 recalls

Product NDC68462-680

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Glenmark Pharmaceuticals Inc. USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205006
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
68462-680-101000 TABLET, FILM COATED in 1 BOTTLE (68462-680-10)Mar 18, 2022
68462-680-3030 TABLET, FILM COATED in 1 BOTTLE (68462-680-30)Mar 18, 2022
68462-680-6060 TABLET, FILM COATED in 1 BOTTLE (68462-680-60)Mar 18, 2022

Recalls mentioning this NDC

Other Lacosamide products