FDA Drug/Biologics Approval BLA 125104, NATALIZUMAB
FDA Drug/Biologics Approval BLA 125104, NATALIZUMAB
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BLA 125104
Company: BIOGEN IDEC
Drug Name: TYSABRI
Active Ingredients: NATALIZUMAB
Strength: 300MG
Dosage Form/Route: VIAL; SINGLE-USE
Action Date: 11/23/2004
Marketing Status: Prescription
Submission Classification: ORIG-1
Company: BIOGEN IDEC
Drug Name: TYSABRI
Active Ingredients: NATALIZUMAB
Strength: 300MG
Dosage Form/Route: VIAL; SINGLE-USE
Action Date: 11/23/2004
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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