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FOIA Request – ANDA Tentative Approval Letter (Amneal EU Ltd, ANDA 218862, Rifaximin 550 mg)
FOIA Request – ANDA Tentative Approval Letter (Amneal EU Ltd, ANDA 218862, Rifaximin 550 mg)
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Request Contents: FOIA request for ANDA tentative approval letter: Any FDA letters notifying Amneal EU Ltd (or related entities) of tentative approval for ANDA No. 218862, Rifaximin tablets, 550 mg.
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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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