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FDA Drug Approval, N125409, PERJETA
FDA Drug Approval, N125409, PERJETA
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NDA: 125409
Company: GENENTECH
Drug Name: PERJETA
Active Ingredients: PERTUZUMAB
Strength: 420MG/14ML
Dosage Form/Route: VIAL; SINGLE-USE
Action Date: 06/08/2012
Marketing Status: Prescription
Submission Classification:
Company: GENENTECH
Drug Name: PERJETA
Active Ingredients: PERTUZUMAB
Strength: 420MG/14ML
Dosage Form/Route: VIAL; SINGLE-USE
Action Date: 06/08/2012
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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