NDC 0131-2477 – Vimpat

Lacosamide 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV 1 recall

Product NDC0131-2477

Product details

Brand name
Vimpat
Generic name
lacosamide
Labeler
UCB, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA022253
Marketed since
May 26, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Vimpat →

Package NDC codes (3)

Package NDCDescriptionSince
0131-2477-3560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0131-2477-35)May 26, 2009
0131-2477-606 BLISTER PACK in 1 CARTON (0131-2477-60) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 26, 2009
0131-2477-991 BLISTER PACK in 1 CARTON (0131-2477-99) / 14 TABLET, FILM COATED in 1 BLISTER PACKMay 26, 2009

Recalls mentioning this NDC

Other Vimpat products