FDA ANNUAL REPORT FOR ANDEXXA (NDA BY ASTRAZENECA) RECEIVED 06/30/22

FDA ANNUAL REPORT FOR ANDEXXA (NDA BY ASTRAZENECA) RECEIVED 06/30/22

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Original Request: The annual report submitted by AstraZeneca AB to the FDA for the product: andexxa, Coagulation Factor Xa (Recombinant), Inactivated-zhzo. The annual report is stated to be received by the FDA on 6/30/22.
Tags: Pharma, BLA, 2022
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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