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FDA Drug Approval, N009866, SOLU-CORTEF
FDA Drug Approval, N009866, SOLU-CORTEF
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NDA: 009866
Company: PHARMACIA AND UPJOHN
Drug Name: SOLU-CORTEF
Active Ingredients: HYDROCORTISONE SODIUM SUCCINATE
Strength: INJECTABLE;INJECTION
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: None
Submission Classification: STANDARD
Company: PHARMACIA AND UPJOHN
Drug Name: SOLU-CORTEF
Active Ingredients: HYDROCORTISONE SODIUM SUCCINATE
Strength: INJECTABLE;INJECTION
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: None
Submission Classification: STANDARD
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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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