Sciele Pharma Announces Acceptance By FDA Of sNDA For New Sular Formulation

Atlanta, CA - Sciele Pharma, Inc. recently announced that the U.S. Food & Drug Administration (FDA) has accepted the supplemental New Drug Application (sNDA) for Sciele's new Sular formulation, with a Pharmacy Drug User Fee Act (PDUFA) date of November 2, 2007. The new Sular formulation utilizes SkyePharma's patented Geomatrix technology, which is designed to provide a lower dose of Sular for each of its current doses.

SOURCE: Sciele Pharma, Inc.