- Chongqing Carelife Pharma, a Fosun Pharma subsidiary, received National Medical Products Administration approval for its sodium thiosulfate injection drug registration.
- The approved indication covers cyanide poisoning and poisoning from arsenic, mercury, lead, bismuth and iodine.
- Fosun Pharma said it invested about CNY1.87 million in R&D for the product as of February 2026.
- Yaopharma will manufacture the injection under approval number Guo Yao Zhun Zi H20263637.
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. Shanghai Fosun Pharmaceutical (Group) Co. 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-20260320-12060998), on March 20, 2026, and is solely responsible for the information contained therein.
Comments