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AbbVie Submits Applications for Upadacitinib (RINVOQ®) in Non-Radiographic Axial Spondyloarthritis to U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA)

/PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that it has submitted applications seeking approvals for upadacitinib (RINVOQ®, 15 mg once daily) to the...
United States Thomas Hudson European Commission Drug Administration Exchange Commission European Union

AbbVie Submits Applications for Upadacitinib (RINVOQ®) in Non-Radiographic Axial Spondyloarthritis to U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA)

NORTH CHICAGO, Ill., Jan. 7, 2022 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that it has submitted applications seeking approvals for upadacitinib (RINVOQ®, 15 mg once daily) to the U.S.
United States Thomas Hudson European Commission Drug Administration Exchange Commission European Union
Source: wsiltv.com

Endo International plc: Endo Announces Agreement for Paladin Labs to Commercialize SK Biopharmaceuticals' XCOPRI (Cenobamate) in Canada

DUBLIN, Dec. 23, 2021 /PRNewswire/ -- Endo International plc (NASDAQ: ENDP) announced today that its subsidiary Endo Ventures Limited has entered into definitive agreements with SK Biopharmaceuticals
Prnewswire Endo International Paladin Labs Inc European Commission Drug Administration Exchange Commission Endo International

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