Core Viewpoint - Zhejiang Jiuzhou Pharmaceutical Co., Ltd. has received a drug registration certificate for Tanshinone IIA from the National Medical Products Administration, which enhances its product pipeline and market competitiveness [1][3]. Drug Basic Information - The drug name is Tanshinone IIA, available in tablet form with specifications of 60mg and 30mg [1]. - It is classified as a Class 4 chemical drug with registration numbers H20255929 and H20255930, valid until November 11, 2030 [1]. - The drug is produced by Jiuzhou Biopharmaceutical (Taizhou) Co., Ltd., located in Taizhou, Zhejiang Province [1]. Market Context - Tanshinone IIA is an oral anticoagulant primarily used for preventing strokes and systemic embolism in patients with non-valvular atrial fibrillation, as well as treating or preventing deep vein thrombosis and pulmonary embolism [2]. - The drug was first developed by Daiichi Sankyo in Japan and launched in April 2011 [2]. - In 2023, the sales revenue of Tanshinone IIA in domestic sample hospitals and pharmacies was approximately RMB 361 million [2]. - The company has invested about RMB 14.41 million in the research and development of Tanshinone IIA [2]. Impact on the Company - The acquisition of the drug registration certificate for Tanshinone IIA will enrich the company's product pipeline and enhance its market competitiveness [3]. - However, this development is not expected to have a significant short-term impact on the company's performance [3].
浙江九洲药业股份有限公司关于全资子公司获得药品注册证书的公告