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FDA Drug Approval, N125377, YERVOY
FDA Drug Approval, N125377, YERVOY
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NDA: 125377
Company: BRISTOL MYERS SQUIBB
Drug Name: YERVOY
Active Ingredients: IPILIMUMAB
Strength: 3MG
Dosage Form/Route: INJECTABLE; INJECTION
Action Date: 03/25/2011
Marketing Status: Prescription
Submission Classification:
Company: BRISTOL MYERS SQUIBB
Drug Name: YERVOY
Active Ingredients: IPILIMUMAB
Strength: 3MG
Dosage Form/Route: INJECTABLE; INJECTION
Action Date: 03/25/2011
Marketing Status: Prescription
Submission Classification:
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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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