NDC 60687-698 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC60687-698

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214695
Marketed since
June 3, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
60687-698-5760 BLISTER PACK in 1 CARTON (60687-698-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-698-11)Jun 3, 2022

Other Lacosamide products