Wyeth Pharmaceuticals And Solvay Pharmaceuticals, Inc. Announce Receipt Of An FDA Action Letter For Bifeprunox
Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), and Solvay Pharmaceuticals, Inc. announced today the receipt of an action letter from the U.S. Food and Drug Administration (FDA) in response to the New Drug Application (NDA) for bifeprunox, an atypical antipsychotic that was reviewed for the acute treatment of schizophrenia, as well as the maintenance of stable adult patients. The Agency stated that the drug was not approvable at this time.
