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Cephalon, Inc. announced receipt of a Paragraph IV Certification Notice Letter on October, 2009 regarding an Abbreviated New Drug Application submitted to the U.S. Food and Drug Administration by Teva Pharmaceuticals USA, Inc. requesting approval to market and sell a generic version of the 50 mg, 100 mg, 150 mg, 200 mg and 250 mg strengths of NUVIGIL Tablets.

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