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Watson Pharmaceuticals, Inc. , a leading specialty pharmaceutical company, announced today that it received a Complete Response Letter from the U.S. Food and Drug Administration on its New Drug Application for TRELSTAR 22.5 mg, a 24-week formulation of TRELSTAR for the palliative treatment of advanced prostate cancer. The TRELSTAR NDA was prepared in cooperation with Debiopharm Group, a Swiss-based global biopharmaceutical group of companies.

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