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FDA Internal Documents – Paraxanthine
FDA Internal Documents – Paraxanthine
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Original Request: Please provide disclosable portions of all internal documents from January 1, 2019 through the present regarding the caffeine metabolite paraxanthine, including, but not limited to, the FDA’s position on its safety, side effect profile, adverse events, and studies. Please provide the documents electronically if possible.
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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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