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NORTH CHICAGO, Ill., July 16, 2021 /PRNewswire/ — AbbVie (NYSE: ABBV) today announced the U.S. Food and Drug Administration (FDA) did not meet the Prescription Drug User Fee Act (PDUFA) action date for the supplemental New Drug Application (sNDA) for RINVOQ® (upadacitinib) for the treatment of adults and adolescents with moderate to severe atopic dermatitis.
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