NDC 0121-1012 – Lacosamide

Lacosamide 50 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CV

Product NDC0121-1012

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA216151
Marketed since
August 26, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
0121-1012-951 TRAY in 1 CASE (0121-1012-95) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1012-05)Apr 28, 2023

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