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FDA Drug/Biologics Approval BLA 103780 S-5121, INTERFERON BETA-1A
FDA Drug/Biologics Approval BLA 103780 S-5121, INTERFERON BETA-1A
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BLA 103780 S-5121
Company: SERONO INC
Drug Name: REBIF
Active Ingredients: INTERFERON BETA-1A
Strength: 44UG/0.5ML
Dosage Form/Route: SYRINGE
Action Date: 03/07/2002
Marketing Status: Prescription
Submission Classification: ORIG-1
Company: SERONO INC
Drug Name: REBIF
Active Ingredients: INTERFERON BETA-1A
Strength: 44UG/0.5ML
Dosage Form/Route: SYRINGE
Action Date: 03/07/2002
Marketing Status: Prescription
Submission Classification: ORIG-1
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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