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Questcor Reports Solid Fourth Quarter Results
Date:3/1/2010

On December 23, 2009 the FDA accepted for review Questcor's supplemental New Drug Application (sNDA) seeking approval to market Acthar for the treatment of infantile spasms.   The FDA has notified Questcor that an Advisory Committee Meeting of independent experts will be held to discuss the approval and use of Acthar in infantile spasms.  The FDA has also notified Questcor that it has set a PDUFA goal date of June 11, 2010, but there is no assurance that this date will not be delayed.  Approval of the IS indication would allow Questcor to promote the use of Acthar in treating IS to child neurologists.  

Previously, the FDA granted Orphan Designation to Acthar for the treatment of IS.  As a result of this Orphan Designation, if Questcor is successful in obtaining FDA approval for the IS indication, Questcor believes that it will also qualify for a seven-year exclusivity period during which the FDA is prohibited from approving any other adrenocorticotropic hormone (ACTH) formulation for IS unless the other formulation is demonstrated to be clinically superior to Acthar.

Cash, Accounts Receivable and Share Repurchase Program

At February 26, 2010, Questcor's cash, cash equivalent
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SOURCE Questcor Pharmaceuticals, Inc.
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