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Purdue Pharmaceutical Products L.P. and Transcept Pharmaceuticals, Inc. announced entry into an exclusive license and collaboration agreement to commercialize Intermezzo in the United States. If approved by the U.S. Food and Drug Administration, Intermezzo has the potential to be the first prescription sleep aid specifically approved for use in the middle of the night at the time a patient awakens and has difficulty returning to sleep. The FDA has established October 2009 as the Prescription Drug User Fee Act action date for the Intermezzo New Drug Application.

 

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