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Pfizer Announces Submission of New Drug Application to the U S FDA for PAXLOVID

30.06.2022 - Pfizer Inc. (NYSE: PFE) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for approval of PAXLOVID (nirmatrelvir [PF-07321332] tablets and ritonavir tablets) for patients who are at high .

From Positive to Negative to Positive Again—The Mystery of Why COVID-19 Rebounds in Some Patients Who Take Paxlovid | Infectious Diseases | JAMA

Pfizer Reports Additional Data on PAXLOVID™ Supporting Upcoming New Drug Application Submission to U S FDA

Pfizer Reports Additional Data on PAXLOVID™ Supporting Upcoming New Drug Application Submission to U S FDA
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