NDC 31722-815 – Lacosamide

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

Human Prescription Drug DEA schedule CV 1 recall

Product NDC31722-815

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Camber Pharmaceuticals, Inc.
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 (4)

Package NDCDescriptionSince
31722-815-05500 TABLET, FILM COATED in 1 BOTTLE (31722-815-05)Mar 17, 2022
31722-815-18180 TABLET, FILM COATED in 1 BOTTLE (31722-815-18)Mar 17, 2022
31722-815-32100 TABLET, FILM COATED in 1 BLISTER PACK (31722-815-32)Mar 17, 2022
31722-815-6060 TABLET, FILM COATED in 1 BOTTLE (31722-815-60)Mar 17, 2022

Recalls mentioning this NDC

Other Lacosamide products