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Salix Pharmaceuticals Ltd announces FDA assigns Sept. 29, Prescription Drug User Fee Act Goal Date for RELISTOR


Monday, 11 Aug 2014 07:00am EDT 

Salix Pharmaceuticals Ltd:Food and Drug Administration (FDA or Agency) has informed Salix that supplemental New Drug Application (sNDA) for RELISTOR(methylnaltrexone bromide) Subcutaneous Injection, 20 mg/ml.Says for treatment of opioid-induced constipation (OIC) in patients taking opioids for chronic non-cancer pain has been assigned user fee goal date of Sept. 29. 

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