CF PharmTech Budesonide Nasal Spray Marketing Application Accepted by NMPA

Reuters01-30
CF PharmTech Budesonide Nasal Spray Marketing Application Accepted by NMPA

CF PharmTech, Inc. announced that its marketing authorization application for budesonide nasal spray has been accepted by the National Medical Products Administration (NMPA) of the People's Republic of China. The application covers budesonide nasal spray in two specifications: 32μg per spray (120 sprays per bottle) and 64μg per spray (120 sprays per bottle), indicated for the treatment of seasonal and perennial allergic rhinitis. The company emphasized that acceptance of the application is an administrative step and does not constitute marketing approval, with further review and assessment by the NMPA pending. There is no assurance that the application will ultimately be approved.

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