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FDA Drug Approval, N020091, IMAGENT
FDA Drug Approval, N020091, IMAGENT
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NDA: 020091
Company: ALLIANCE PHARM
Drug Name: IMAGENT
Active Ingredients: PERFLUBRON
Strength: 100%
Dosage Form/Route: LIQUID;ORAL
Action Date: 08/13/1993
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
Company: ALLIANCE PHARM
Drug Name: IMAGENT
Active Ingredients: PERFLUBRON
Strength: 100%
Dosage Form/Route: LIQUID;ORAL
Action Date: 08/13/1993
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
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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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