Fusen Pharmaceutical Wins Regulatory Approval for Nicardipine Hydrochloride Injection in China

Reuters
12/12
Fusen Pharmaceutical Wins Regulatory Approval for Nicardipine Hydrochloride Injection in China

Fusen Pharmaceutical Company Limited has announced that it has received regulatory approval from the National Medical Products Administration of the PRC for the consistency evaluation of its Nicardipine Hydrochloride Injection. Developed by its wholly-owned subsidiary, Henan Fusen Pharmaceutical Company Limited, this product is intended for the emergency management of perioperative hypertension and hypertensive emergencies. The approval covers multiple specifications, including 2ml:2mg, 5ml:5mg, and 10ml:10mg, making Fusen one of the companies in China with the most comprehensive range of this product. No grant or funding from multiple organizations was mentioned.

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. Fusen Pharmaceutical Company 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-20251212-11954475), on December 12, 2025, and is solely responsible for the information contained therein.

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