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FDA Approval Letter & Product Label – PROMACTA (Eltrombopag Olamine) for Litigation in India (Certified Copies)
FDA Approval Letter & Product Label – PROMACTA (Eltrombopag Olamine) for Litigation in India (Certified Copies)
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Original Request Contents: Certified copies of FDA approval letter and product label for PROMACTA (eltrombopag olamine) for litigation in India (see attached PDF for details and template certificate)
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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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