Salix Stock Slammed on Word of CRL for Xifaxan
By Marie Powers
Friday, February 25, 2011
Salix Pharmaceuticals Ltd. delivered bad news to investors Thursday morning. Based on a phone call with the FDA Wednesday evening, the Raleigh, N.C.-based company now expects to receive a complete response letter (CRL) on its supplemental new drug application (sNDA) for Xifaxan (rifaximin) 550-mg tablets for the treatment of non-constipation irritable bowel syndrome (non-CIBS) and IBS-related bloating.
Outside of the US
Part of Thomson Reuters
Note: our contact information has changed
In the U.S. and Canada: +1-800-336-4474
Outside the U.S.: +44-203-684-1796
Hours: Monday - Friday, 8:00am - 6:00 pm EST
© 2017 Thomson Reuters. Reproduction, reposting content is strictly prohibited.