FDA Drug/Biologics Approval BLA 125504 S-002, SECUKINUMAB
FDA Drug/Biologics Approval BLA 125504 S-002, SECUKINUMAB
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BLA 125504 S-002
Company: NOVARTIS PHARMS CORP
Drug Name: COSENTYX
Active Ingredients: SECUKINUMAB
Strength: 150MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 01/21/2015
Marketing Status: Prescription
Submission Classification: ORIG-1
Company: NOVARTIS PHARMS CORP
Drug Name: COSENTYX
Active Ingredients: SECUKINUMAB
Strength: 150MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 01/21/2015
Marketing Status: Prescription
Submission Classification: ORIG-1
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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