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FDA Drug Approval, A088703, PREDNISONE
FDA Drug Approval, A088703, PREDNISONE
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ANDA: 088703
Company: HIKMA
Drug Name: PREDNISONE
Active Ingredients: PREDNISONE
Strength: 5MG/5ML
Dosage Form/Route: SOLUTION;ORAL
Action Date: 11/08/1984
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: None
Company: HIKMA
Drug Name: PREDNISONE
Active Ingredients: PREDNISONE
Strength: 5MG/5ML
Dosage Form/Route: SOLUTION;ORAL
Action Date: 11/08/1984
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: None
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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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