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FDA Drug/Biologics Approval BLA 761083 S-004, EMICIZUMAB
FDA Drug/Biologics Approval BLA 761083 S-004, EMICIZUMAB
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BLA 761083 S-004
Company: GENENTECH INC
Drug Name: HEMLIBRA
Active Ingredients: EMICIZUMAB
Strength: 150MG
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 11/16/2017
Marketing Status: Prescription
Submission Classification: ORIG-1
Company: GENENTECH INC
Drug Name: HEMLIBRA
Active Ingredients: EMICIZUMAB
Strength: 150MG
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 11/16/2017
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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