CSPC Pharmaceutical Group Receives Approval for Clevidipine Injectable Emulsion

Reuters02-02 19:53

CSPC Pharmaceutical Group Receives Approval for Clevidipine Injectable Emulsion

CSPC Pharmaceutical Group Limited announced that its Clevidipine Injectable Emulsion (50ml:25mg, 100ml:50mg) has obtained drug registration approval from the National Medical Products Administration of the People's Republic of China. Clevidipine Injectable Emulsion is a dihydropyridine calcium channel blocker indicated for the treatment of patients with hypertension when oral therapy is not feasible or is anticipated to be ineffective. The product offers a rapid onset of action, does not require dose adjustment for patients with hepatic or renal dysfunction, and can be administered without dilution, making it suitable for patients at risk of fluid overload. This approval is expected to strengthen the company's product pipeline in the cardiovascular therapeutic area.

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. CSPC Pharmaceutical 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-20260202-12009836), on February 02, 2026, and is solely responsible for the information contained therein.

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