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FDA Registration & Supplements – Prednisolone Acetate Ophthalmic 216935
FDA Registration & Supplements – Prednisolone Acetate Ophthalmic 216935
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Original Request: Product registration documentation and any subsequent supplements for the Prednisilone acetate Opthalmic suspension/drops 216935
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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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