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Sucampo’s Amitiza Review Period Set

02/23/2007

Federal Register Notice FDA has determined the regulatory review period for Sucampo AG’s Amitiza is 2,197 days for the extension of a patent which claims the human drug product. Amitiza (lubiprostone) is indicated for treating chronic idiopathic constipation in the adult population. To view this notice, click here.

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