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.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. CF Pharmtech Inc. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260130-12005352), on January 29, 2026, and is solely responsible for the information contained therein.
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