NDC 60687-676 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC60687-676

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 1, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
60687-676-5760 BLISTER PACK in 1 CARTON (60687-676-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-676-11)Jun 1, 2022

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