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FDA CDRH Intercenter Consult Memorandum – FUROSCIX NDA 209988, including Label, Labeling, and Human Factors Results Review.
FDA CDRH Intercenter Consult Memorandum – FUROSCIX NDA 209988, including Label, Labeling, and Human Factors Results Review.
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Original Request: CDRH INTERCENTER CONSULT MEMORANDUM and LABEL, LABELING AND HUMAN FACTORS RESULTS REVIEW from the Division of Medication Error Prevention and Analysis (DMEPA) from the FUROSCIX NDA 209988 (80MG/10ML (8MG/ML) SOLUTION;SUBCUTANEOUS)
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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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