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  • FDA Grants Priority Review of 10 mg XARELTO to Reduce VTE Risk americanpharmaceuticalreview
    June 29, 2017
    Janssen Research & Development announced the U.S. Food and Drug Administration (FDA) accepted for Priority Review a supplemental New Drug Application (sNDA) for XARELTO (rivaroxaban) to include a 10 mg once-daily dose for reducing the risk of VTE after at

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