US FDA declines to approve Orexo's opioid overdose drug
July 16 (Reuters) - The U.S. Food and Drug Administration has declined to approve Orexo AB's ORX.ST high-dose prescription drug for opioid overdose, the company said on Tuesday. (Reporting by Vallari Srivastava, Sriparna Roy and Unnamalai L in Bengaluru; Editing by Tasim Zahid) ((Sriparna.Roy@thomsonreuters.com;))
Recent news on Orexo AB
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Sweden's Orexo Q1 revenue drops, net loss widens