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Cephalon, Inc. (Nasdaq: CEPH) proclaimed that the U.S. Food and Drug Administration (FDA) has extensive the fulfill escort to March 29, 2010, for its follow-up of the supplementary New Drug Application (sNDA) for NUVIGIL ® (armodafinil) Tablets [C-IV]. The sNDA is for the indicant of improved vigilance in patients with exuberant drowsiness associated with jet lag cark due to eastward locomotion.