• Purdue Pharma seeks FDA authorization to market once-daily hydrocodone bitartrate tablet

    by  • 30 April 2014 • Pain News

    Purdue Pharma L.P. announced that it has filed a New Drug Application (NDA) with the U.S. Food & Drug Administration seeking authorization to market a once-daily, single-entity hydrocodone bitartrate tablet (HYD).


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