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FDA Drug Approval, N017243, ULTRA-TECHNEKOW FM
FDA Drug Approval, N017243, ULTRA-TECHNEKOW FM
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NDA: 017243
Company: CURIUM
Drug Name: ULTRA-TECHNEKOW FM
Active Ingredients: TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR
Strength: 1-19 CI/GENERATOR
Dosage Form/Route: SOLUTION;INTRAVENOUS
Action Date: 11/23/1973
Marketing Status: Prescription
Submission Classification: Type 5 - New Formulation or New Manufacturer
Company: CURIUM
Drug Name: ULTRA-TECHNEKOW FM
Active Ingredients: TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR
Strength: 1-19 CI/GENERATOR
Dosage Form/Route: SOLUTION;INTRAVENOUS
Action Date: 11/23/1973
Marketing Status: Prescription
Submission Classification: Type 5 - New Formulation or New Manufacturer
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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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