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FDA Drug/Biologics Approval BLA 125156 S-106, RANIBIZUMAB
FDA Drug/Biologics Approval BLA 125156 S-106, RANIBIZUMAB
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BLA 125156 S-106
Company: GENENTECH
Drug Name: LUCENTIS
Active Ingredients: RANIBIZUMAB
Strength: 6MG/ML
Dosage Form/Route: Injectable; Injection
Action Date: 06/30/2006
Marketing Status: Prescription
Submission Classification: ORIG-1
Company: GENENTECH
Drug Name: LUCENTIS
Active Ingredients: RANIBIZUMAB
Strength: 6MG/ML
Dosage Form/Route: Injectable; Injection
Action Date: 06/30/2006
Marketing Status: Prescription
Submission Classification: ORIG-1
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- 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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