NDC 67877-736 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC67877-736

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214695
Marketed since
April 1, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (4)

Package NDCDescriptionSince
67877-736-05500 TABLET, FILM COATED in 1 BOTTLE (67877-736-05)Apr 1, 2022
67877-736-316 BLISTER PACK in 1 CARTON (67877-736-31) / 10 TABLET, FILM COATED in 1 BLISTER PACKApr 1, 2022
67877-736-6060 TABLET, FILM COATED in 1 BOTTLE (67877-736-60)Apr 1, 2022
67877-736-9090 TABLET, FILM COATED in 1 BOTTLE (67877-736-90)Apr 1, 2022

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