Group 1 - The company Shanghai Pharmaceutical Group Co., Ltd. announced that its subsidiary, Shanghai Xinyi Jinzhu Pharmaceutical Co., Ltd., received a notification from the National Medical Products Administration approving the supplementary application for the drug Dihydroxypropyl Theophylline Injection, which has passed the consistency evaluation of quality and efficacy for generic drugs [1][2] - The drug Dihydroxypropyl Theophylline Injection is indicated for bronchial asthma, wheezing bronchitis, and obstructive pulmonary emphysema, and it was developed by Eisai Co., Ltd. and launched in Japan in October 1952 [2] - As of the announcement date, the company has invested approximately RMB 3.05 million in research and development for this drug [2] Group 2 - The approval of the drug's consistency evaluation is expected to enhance its market share and competitiveness, as products that pass this evaluation will receive greater support in medical insurance payments and procurement by medical institutions [2] - The total procurement amount for Dihydroxypropyl Theophylline Injection (2ml:0.3g) in hospitals in mainland China for 2024 is reported to be RMB 9.737 million [2]

Group 1 - The core point of the article is that Shanghai Pharmaceuticals announced the approval of its dihydroxypropyl theophylline injection by the National Medical Products Administration, indicating that the drug has passed the consistency evaluation of quality and efficacy for generic drugs [2] Group 2 - The drug is produced by Shanghai Xinyi Jinzhu Pharmaceutical Co., Ltd., a subsidiary of Shanghai Pharmaceuticals [2] - The approval signifies a significant milestone for the company in expanding its product portfolio in the pharmaceutical market [2] - The consistency evaluation is crucial for ensuring that generic drugs meet the same standards as their branded counterparts, which can enhance market competitiveness [2]

Core Viewpoint - Shanghai Pharmaceuticals has received approval for its Dihydroxypropyl Theophylline Injection from the National Medical Products Administration, indicating successful completion of the consistency evaluation for generic drug quality and efficacy [1] Company Summary - Shanghai Pharmaceuticals' subsidiary, Shanghai Xinyi Jinzhu Pharmaceutical Co., Ltd., is responsible for the Dihydroxypropyl Theophylline Injection [1] - The approval was granted through a supplementary application, with the notification number 2025B04012 [1] - The drug has passed the consistency evaluation for quality and efficacy as a generic medication [1]

Core Viewpoint - Shanghai Pharmaceuticals has received approval for its Dihydroxypropyl Theophylline Injection from the National Medical Products Administration, indicating successful consistency evaluation for generic drug quality and efficacy [1] Group 1: Company Developments - Shanghai Pharmaceuticals' subsidiary, Shanghai Xinyi Jinzhu Pharmaceutical Co., Ltd., has been granted a Supplementary Application Approval Notice for Dihydroxypropyl Theophylline Injection [1] - The drug is indicated for bronchial asthma, asthmatic bronchitis, obstructive pulmonary emphysema, and symptoms of dyspnea due to cardiogenic pulmonary edema [1] - The company has invested approximately RMB 3.05 million in research and development for this drug as of the announcement date [1] Group 2: Market Insights - According to IQVIA data, the procurement amount for Dihydroxypropyl Theophylline Injection (2ml: 0.3g) in hospitals across mainland China for 2024 is RMB 9.737 million [2] - Major domestic manufacturers of this drug include Jilin Jingsheng Pharmaceutical Co., Shanxi Taiyuan Pharmaceutical Co., and Suicheng Pharmaceutical Co., Ltd. [1]

香港交易及結算所有限公司和香港聯合交易所有限公司對本公告的內容概不負責，對其準確性 或完整性亦不發表任何聲明，並明確表示，概不對因本公告全部或任何部分內容而產生或因依賴 該等內容而引致的任何損失承擔任何責任。 上 海 醫 藥 集 團 股 份 有 限 公 司 Shanghai Pharmaceuticals Holding Co., Ltd. * （於中華人民共和國註冊成立的股份有限公司） （股份代碼：02607） 海外監管公告 本公告乃根據香港聯合交易所有限公司證券上市規則第 13.10B 條而作出。 茲載列上海醫藥集團股份有限公司（「本公司」）在上海證券交易所網站(http://www.sse.com.cn) 刊登的《上海醫藥集團股份有限公司關於二羥丙茶鹼注射液通過仿製藥一致性評價的公告》 僅供參閱。 承董事會命 上海醫藥集團股份有限公司 楊秋華 董事長 中國上海，2025 年 9 月 5 日 於本公告日期，本公司的執行董事為楊秋華先生、沈波先生、李永忠先生及董明 先生；非執行董事為張文學先生；以及獨立非執行董事為顧朝陽先生、霍文遜先 生、王忠先生及萬鈞女士。 * 僅供識別 证券代码：601607 证券简称 ...

Core Viewpoint - Shanghai Pharmaceuticals announced the approval of its Dihydroxypropyl Theophylline Injection by the National Medical Products Administration, indicating successful compliance with the consistency evaluation of generic drug quality and efficacy [1] Company Summary - Shanghai Pharmaceuticals' subsidiary, Shanghai Xinyi Jinzhu Pharmaceutical Co., Ltd., received the approval notification for Dihydroxypropyl Theophylline Injection [1] - The injection is indicated for the relief of symptoms in bronchial asthma, asthmatic bronchitis, obstructive pulmonary emphysema, and can also be used for wheezing due to cardiogenic pulmonary edema [1]

Core Viewpoint - Goldman Sachs reported that Shanghai Pharmaceuticals (02607) had a second-quarter sales of 70.8 billion RMB, a year-on-year increase of 2.3%, which was below expectations, indicating continued weakness across various market segments [1] Financial Performance - The second-quarter recurring net profit was consistent with well-controlled expenditures, but was partially offset by a decline in gross margin [1] - The decline in gross margin was primarily attributed to the ongoing decrease in manufacturing profit margins [1] Earnings Forecast - Goldman Sachs adjusted the company's earnings forecasts for this year, next year, and 2027 to an increase of 33.5%, a decrease of 0.3%, and a decrease of 6.4%, respectively [1] - The target price was lowered from 10.29 HKD to 10.08 HKD, maintaining a "Sell" rating [1]

Core Viewpoint - Goldman Sachs reports that Shanghai Pharmaceuticals (601607)(02607) experienced a second-quarter sales revenue of 70.8 billion RMB, a year-on-year increase of 2.3%, which is below expectations, indicating continued weakness across various market segments [1] Financial Performance - The second-quarter recurring net profit was consistent with well-controlled expenditures, but was partially offset by a decline in gross margin [1] - The decline in gross margin is primarily attributed to the ongoing decrease in manufacturing profit margins [1] Earnings Forecast - The company’s earnings forecasts for this year, next year, and 2027 have been adjusted to an increase of 33.5%, a decrease of 0.3%, and a decrease of 6.4%, respectively [1] - The target price has been lowered from 10.29 HKD to 10.08 HKD, while maintaining a "Sell" rating [1]

证券代码：601607 证券简称：上海医药 编号：临 2025-081 上海医药集团股份有限公司 关于二羟丙茶碱注射液通过仿制药一致性评价的公告 本公司董事会及全体董事保证本公告内容不存在任何虚假记载、误导性陈述 或者重大遗漏，并对其内容的真实性、准确性和完整性承担个别及连带责任。 近日，上海医药集团股份有限公司（以下简称"公司"）下属上海信谊金朱 药业有限公司（以下简称"信谊金朱"）的二羟丙茶碱注射液（以下简称"该药 品"）收到国家药品监督管理局（以下简称"国家药监局"）颁发的《药品补充 申请批准通知书》（通知书编号：2025B04012），该药品通过仿制药质量和疗 效一致性评价。 一、该药品基本情况 药物名称：二羟丙茶碱注射液 剂型：注射剂 规格：2ml:0.3g 注册分类：化学药品 药品批准文号：国药准字 H20258173 申请人：上海信谊金朱药业有限公司 审批结论：批准本品增加 2ml:0.3g 规格的补充申请，核发药品批准文号，本 品通过仿制药质量和疗效一致性评价。 二、该药品相关的信息 二羟丙茶碱注射液适用于支气管哮喘、喘息型支气管炎、阻塞性肺气肿等缓 解喘息症状。也可用于因心源性肺水肿而致的喘 ...

Core Viewpoint - Shanghai Pharmaceuticals (601607) announced that its subsidiary, Shanghai Xinyi Jinzhu Pharmaceutical Co., Ltd., received the approval notice from the National Medical Products Administration for its Dihydrocodeine Injection, which has passed the consistency evaluation of quality and efficacy for generic drugs [1] Group 1 - The Dihydrocodeine Injection is indicated for the relief of symptoms in bronchial asthma, asthmatic bronchitis, and obstructive pulmonary emphysema [1] - The drug can also be used for alleviating symptoms caused by pulmonary edema due to heart disease [1]