Cephalon Receives FDA Approval for TREANDA to Treat Patients with Relapsed Indolent Non-Hodgkin’s Lymphoma (PR Newswire via Yahoo! Finance)

Cephalon, Inc., today announced that the U.S. Food and Drug Administration has approved TREANDA® for Injection for the treatment of patients with indolent B-cell non-Hodgkin's lymphoma that has progressed during or within six months of treatment with rituximab or a rituximab-containing regimen.

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