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FDA Packaging Insert & Labeling – Hydrocortisone Sodium Phosphate (RTU) Injection 50 MG BASE/ML (Discontinued; NDA 012052, MERCK AND CO INC)
FDA Packaging Insert & Labeling – Hydrocortisone Sodium Phosphate (RTU) Injection 50 MG BASE/ML (Discontinued; NDA 012052, MERCK AND CO INC)
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Original Request Contents: Packaging insert and labeling for Hydrocortisone Sodium Phosphate (RTU) injection – 50MG BASE/ML, discontinued; NDA 012052, Applicant: MERCK AND CO INC
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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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