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    1/8/2009 - Ipsen: FDA's First-Cycle Review Of Reloxin(R) Extended
    Posted in Medical News

    Ipsen (Paris:IPN) announced that the U.S. Food and Drug patronage (FDA) on order notification that the formula Drug User Fee Act (PDUFA) action date for Reloxin® (botulinum toxin of type A) Biologics License form (BLA) in aesthetic indications (glabellar lines) has been broad to April 13, 2009. The FDA did not issue any express request on the occurrence of this extension.

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