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FDA Drug/Biologics Approval BLA 103172 S-5003, ALTEPLASE
FDA Drug/Biologics Approval BLA 103172 S-5003, ALTEPLASE
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BLA 103172 S-5003
Company: GENENTECH
Drug Name: CATHFLO ACTIVASE
Active Ingredients: ALTEPLASE
Strength: 2MG/VIAL
Dosage Form/Route: VIAL
Action Date: 11/13/1987
Marketing Status: Prescription
Submission Classification: ORIG-1
Company: GENENTECH
Drug Name: CATHFLO ACTIVASE
Active Ingredients: ALTEPLASE
Strength: 2MG/VIAL
Dosage Form/Route: VIAL
Action Date: 11/13/1987
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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