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FDA Drug Approval, N017011, PRED FORTE
FDA Drug Approval, N017011, PRED FORTE
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NDA: 017011
Company: ABBVIE
Drug Name: PRED FORTE
Active Ingredients: PREDNISOLONE ACETATE
Strength: SUSPENSION/DROPS;OPHTHALMIC
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: AB
Submission Classification: STANDARD
Company: ABBVIE
Drug Name: PRED FORTE
Active Ingredients: PREDNISOLONE ACETATE
Strength: SUSPENSION/DROPS;OPHTHALMIC
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: AB
Submission Classification: STANDARD
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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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