China Accepts Luye Pharma's NDA for Ruoxinlin in Generalized Anxiety Disorder

Reuters01-08

China Accepts <a href="https://laohu8.com/S/LYPHF">Luye Pharma</a>'s NDA for Ruoxinlin in Generalized Anxiety Disorder

Luye Pharma Group Ltd. has announced that the Centre for Drug Evaluation of the National Medical Products Administration in China has accepted the New Drug Application for a new indication of Ruoxinlin® (Toludesvenlafaxine Hydrochloride Sustained-Release Tablets) for the treatment of Generalized Anxiety Disorder. This application marks a significant milestone for Ruoxinlin®, which was previously approved in November 2022 for the treatment of Major Depressive Disorder.

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. Luye Pharma Group Ltd. 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-20260108-11985249), on January 08, 2026, and is solely responsible for the information contained therein.

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