NDC 16714-552 – Lacosamide

Lacosamide 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CV

Product NDC16714-552

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
NorthStar RxLLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208308
Marketed since
August 1, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
16714-552-0160 TABLET in 1 BOTTLE (16714-552-01)Aug 1, 2022

Other Lacosamide products