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FDA Summary Basis of Approval – SOLU‑MEDROL NDA N011856 & SOLU‑CORTEF NDA N009866
FDA Summary Basis of Approval – SOLU‑MEDROL NDA N011856 & SOLU‑CORTEF NDA N009866
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Original Request Contents: SBOA for SOLU‑MEDROL (Methylprednisolone Sodium Succinate for Injection) NDA N011856 and for SOLU‑CORTEF (Hydrocortisone Sodium Succinate for Injection) NDA N009866
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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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