Drugplain

NDC 71921-222-06

Lacosamide 150 mg/1

Lacosamide · TABLET

No Recall History

Lacosamide is a tablet containing lacosamide at a strength of 150 mg/1. Manufactured by Florida Pharmaceutical Products, LLC.

Key Facts

Brand Name
Lacosamide
Generic Name
Lacosamide
NDC Code (Package)
71921-222-06
NDC Code (Product)
71921-222
Manufacturer
Florida Pharmaceutical Products, LLC
Strength
150 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
DEA Schedule
Schedule V (Controlled)
Application #
ANDA208308
Marketing Start
09/21/2023

Recall History

No Recall History

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Lacosamide — All Packages

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.