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Entreprise · 25/02/20021 min de lecture
Determination of Regulatory Review Period for Purposes of Patent Extension; Celexa
Traduction automatique locale · Langue originale de la source
Résumé
The Food and Drug Administration (FDA) has determined the regulatory review period for Celexa and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Commissioner of Patents and Trademarks, Department of Commerce, for the extension of a patent that claims that human drug product.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →