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Negócios · 15/05/20081 min de leitura
Determination of Regulatory Review Period for Purposes of Patent Extension; TYZEKA
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Resumo
The Food and Drug Administration (FDA) has determined the regulatory review period for TYZEKA and is publishing this notice of that determination as required by law. FDA has made the determination because of the submissions of applications to the Director of Patents and Trademarks, Department of Commerce, for the extension of patents which claim that human drug product.
Idioma original da fonte: Federal Register — Food and Drug AdministrationAbrir o comunicado original →