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Generic User Fee Transition A Little Bumpy For Contract Manufacturers

Executive Summary

Problems with self-identification process caused by timing of legislative renewal may have affected figures used by US FDA to calculate FY 2018 GDUFA fees.

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A firm will take ownership of US ANDAs from manufacturers unwilling to pay program fees or withdraw the approved generic drug application; is it a novel concept allowing future marketing options or simply fee avoidance?

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Agency primarily uses application data instead of facility self-identification lists to determine FY 2018 generic drug user fees.

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