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FDA Drug Approval, A206604, FERUMOXYTOL
FDA Drug Approval, A206604, FERUMOXYTOL
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ANDA: 206604
Company: SANDOZ
Drug Name: FERUMOXYTOL
Active Ingredients: FERUMOXYTOL
Strength: EQ 510MG IRON/17ML (EQ 30MG IRON/ML)
Dosage Form/Route: SOLUTION;INTRAVENOUS
Action Date: 01/15/2021
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
Company: SANDOZ
Drug Name: FERUMOXYTOL
Active Ingredients: FERUMOXYTOL
Strength: EQ 510MG IRON/17ML (EQ 30MG IRON/ML)
Dosage Form/Route: SOLUTION;INTRAVENOUS
Action Date: 01/15/2021
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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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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