NDC 71921-220 – Lacosamide

Lacosamide 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CV

Product NDC71921-220

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208308
Marketed since
September 21, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
71921-220-0660 TABLET in 1 BOTTLE (71921-220-06)Sep 21, 2023

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