10月29日，步长制药(603858.SH)披露2025年三季报，前三季度实现营业收入84.69亿元，同比下降 0.54%；归属于上市公司股东的净利润8.68亿元，同比增加177.54%；基本每股收益0.8208元。业绩逆势 增长的背后，是公司在产品创新、国际化布局、技术升级等业务领域的持续突破。 从秦岭脚下的创业初心到遍布全国的产业布局，从单一产品的突破到多领域的协同发展，步长制药三十 余年的成长轨迹中，始终镌刻着"取之于社会，回馈于社会"的价值印记。在追求企业发展的同时，这家 医药企业以持续的公益投入、稳定的分红回报、厚重的纳税贡献，诠释着民营企业的社会责任与时代担 当。 业务突破显实力：前三季度核心动态盘点 步长制药在"以中药为基础，向生物药、疫苗领域扩张"战略指导下，前三季度在产品管线、国际市场、 技术创新与管理体系四大领域密集发力，为高质量发展注入强劲动力。 核心产品再添新证，民生用药布局深化：10月13日，步长制药全资子公司山东丹红制药收到国家药监局 核准签发的布洛芬缓释胶囊《药品注册证书》。作为临床常用的非甾体抗炎药，该产品的获批进一步丰 富了步长制药在解热镇痛领域的产品线，可更好满足基层医疗与 ...

Core Insights - The company reported a gross margin of 77.36% for the first three quarters, showing an improvement from the mid-year report, with a significant increase to 79.03% in the third quarter, indicating sustained profitability momentum [1] - The rise in gross margin reflects the company's strong technical foundation and comprehensive competitive strength in its products [1] - New products such as Celecoxib capsules and Oseltamivir phosphate capsules are rapidly gaining market traction, while prescription drugs have achieved breakthroughs in sales in Northeast China, solidifying the company's performance base [1] R&D and Production Capacity - The company has a robust R&D pipeline that supports its profitability, with clinical trials for innovative drug Maja Zizi capsules progressing steadily and other products like Vornorphan tablets nearing market launch [1] - The company is accelerating production upgrades, with the GMP expansion project in Neijiang initiated in March, leading to a significant increase in "other non-current assets" to 15.61 million, a year-on-year growth of 6565.56% [1] - The second phase of the production facility is expected to be fully completed by 2026, with partial production lines anticipated to be operational by the end of 2025, adding seven new product lines for gel formulations and soft capsules [1] Market Outlook - Open Source Securities expresses optimism regarding the company's R&D project potential and its positioning within the traditional Chinese medicine industry chain, projecting a return on equity (ROE) of 11.7% by 2026 and maintaining a "buy" rating for the company [2]

Core Insights - The integration of medical insurance payment for purchasing medicine through Taobao Flash Purchase has become a new habit for many consumers, with over 40 cities supporting this service and reaching nearly 300 districts and counties [1] - The service significantly enhances consumer experience by providing quick delivery, with medicines delivered in as fast as 19 minutes, addressing urgent medication needs [3] Group 1: Service Coverage and User Experience - Taobao Flash Purchase's online medical insurance drug purchasing service has over 80% coverage in major cities like Shanghai and Shenzhen, with some areas exceeding 98% [3] - The service allows users to easily access medication through the Taobao app or Alipay, significantly reducing the need for physical trips to pharmacies, especially during late hours or adverse weather [5] - Common medications such as cold relief granules and ibuprofen are among the top ordered items through the medical insurance purchasing option [5] Group 2: Market Trends and Future Developments - The service is part of a broader initiative by the National Medical Insurance Administration to enhance convenience in the healthcare sector, promoting "Internet + Medical Services" [8] - Taobao Flash Purchase plans to continue exploring innovative solutions, including AI applications in the drug search process and partnerships with online hospitals for prescription drug purchases [8] - The service is particularly beneficial for elderly customers, as it reduces their need to go out, thus minimizing health risks [7]

格隆汇10月13日丨步长制药(603858.SH)公布，全资子公司山东丹红制药有限公司近日收到国家药品监 督管理局核准签发的关于布洛芬缓释胶囊的《药品注册证书》。布洛芬缓释胶囊适应症：用于缓解轻至 中度疼痛如头痛、关节痛、偏头痛、牙痛、肌肉痛、神经痛、痛经。也用于普通感冒或流行性感冒引起 的发热。 ...

Core Viewpoint - The announcement by the company regarding the approval of Ibuprofen sustained-release capsules by the National Medical Products Administration indicates a significant development in its product portfolio, aimed at addressing various types of pain and fever associated with common illnesses [1] Company Summary - The company, Bicheng Pharmaceutical, has received a drug registration certificate for Ibuprofen sustained-release capsules from the National Medical Products Administration [1] - The approved indication for the drug includes relief from mild to moderate pain such as headaches, joint pain, migraines, toothaches, muscle pain, neuralgia, and dysmenorrhea, as well as fever caused by common colds or influenza [1] Industry Summary - The approval of this medication aligns with the growing demand for effective pain management solutions in the pharmaceutical industry, particularly for over-the-counter medications [1] - The introduction of Ibuprofen sustained-release capsules may enhance competition within the pain relief segment of the pharmaceutical market [1]

南财智讯10月13日电，步长制药公告，公司全资子公司山东丹红制药有限公司近日收到国家药品监督管 理局签发的布洛芬缓释胶囊《药品注册证书》。该产品用于缓解轻至中度疼痛及发热等症状。 ...

Core Viewpoint - The new centralized procurement rules for pharmaceuticals aim to address historical issues and promote sustainable development in the pharmaceutical industry, balancing price control, quality assurance, and supply stability [1][10]. Group 1: Historical Issues and Data - The new procurement rules are designed to resolve past issues such as low-price competition, quality instability, and supply shortages, which have been prevalent since the initiation of the centralized procurement system [2][4]. - The latest round of procurement includes 55 drug varieties across various therapeutic areas, with an average of 15 companies competing for each variety, indicating strong market interest and competition [2][3]. Group 2: Reporting and Supply Assurance - The reporting phase for the latest procurement batch requires medical institutions to submit annual demand volumes that are generally not less than 80% of the average usage from 2023 to 2024, allowing for brand recognition in the reporting process [3][6]. - The new rules designate selected companies as the primary responsible parties for supply assurance, imposing penalties for non-compliance, which aims to reduce the occurrence of supply shortages [3][6]. Group 3: Impact on Pricing and Quality - The optimization of procurement rules is expected to alleviate the pressure on companies that previously relied on extremely low bids, promoting a healthier competitive environment [6][10]. - The new regulations encourage a balance between price and quality, ensuring that patients benefit from affordable medications without compromising on safety and efficacy [7][10]. Group 4: Industry Dynamics and Future Outlook - The changes are likely to accelerate the elimination of weaker players in the pharmaceutical sector, favoring larger, more capable companies that can maintain quality and supply stability [8][10]. - The shift from a price-first approach to one that equally values quality and supply stability is anticipated to enhance public confidence in generic drug quality and support the sustainable development of the healthcare system [10].

Core Viewpoint - There is a significant price discrepancy between online and offline pharmacies for the same medications, with some prices being more than three times higher in physical stores compared to online platforms [1][2][5]. Group 1: Price Discrepancy - A survey of ten pharmacies revealed that the same medication can have a price difference of over three times between online and offline sales [1][6]. - For example, the "仁和" artificial cow bile metronidazole capsules cost 8.68 yuan online but 32 yuan offline, resulting in a difference of 23.32 yuan [1][6]. - Other examples include "可益甘" artificial cow bile metronidazole capsules priced at 5.8 yuan online and 15.8 yuan offline, and "百多邦" mupirocin ointment at 19.2 yuan online versus 23.2 yuan offline [5][6]. Group 2: Reasons for Price Differences - Pharmacy staff indicated that online prices are often lower due to platform subsidies, although not all medications follow this trend [2][9]. - Consumers have the option to choose between online and offline purchases based on their preferences, but online shopping may incur additional delivery fees [2][9]. - Legal experts noted that the price difference alone does not constitute price fraud; it must be assessed in the context of whether the pharmacy transparently communicates the reasons for the price difference [11][12]. Group 3: Regulatory Responses - The National Medical Insurance Administration has issued directives to compare offline pharmacy prices with online platforms to address unreasonable pricing [10]. - Local regulations have been established, such as in Shaanxi Province, where offline prices cannot exceed 20% of the online price displayed by the same pharmacy [10]. - Zhejiang Province has mandated that online prices should not exceed 1.3 times the listed price, emphasizing the need for price consistency across different sales channels [10].

Core Viewpoint - The introduction of self-service medicine vending machines is raising concerns among traditional pharmacies about competition and regulatory compliance, particularly regarding the sale of prescription drugs [5][12][14]. Group 1: Market Trends and Data - The retail pharmacy sector is experiencing a decline in growth, with physical pharmacies projected to see a decrease of 0.4% from 2023 to 2024, following a drop of 0.9% from 2022 to 2023 [3]. - E-commerce B2C channels, including internet hospitals, are showing growth, with a 26.9% increase in 2022 compared to 2021, and an 18.8% increase in 2023 compared to 2022 [4]. - The self-service vending machines can hold over a thousand types of medications and are designed to meet the 24-hour medication needs of consumers, addressing the "last mile" issue in drug purchasing [5][7]. Group 2: Regulatory Environment - The Beijing regulations specify that self-service machines can only sell Class B non-prescription drugs (OTC), which has led to concerns about the potential for these machines to dispense prescription medications without proper oversight [9][10]. - The National Medical Products Administration has stated that self-service machines are not allowed to sell prescription drugs, emphasizing the need for regulatory compliance in the distribution of medications [13]. Group 3: Industry Concerns - Pharmacy operators are worried that self-service machines could operate without licensed pharmacists, leading to potential safety risks in medication dispensing [15][18]. - The operational costs for traditional pharmacies, including the need for licensed pharmacists, are significantly higher compared to the low overhead of self-service machines, which could create an uneven playing field [20][23]. - The rapid deployment of self-service machines could disrupt the traditional pharmacy model, as they can be set up quickly and at a lower cost compared to opening new physical locations [24][26]. Group 4: Economic Implications - The cost of maintaining a licensed pharmacist in a physical pharmacy can add approximately 20,000 yuan per month, while self-service machines do not incur such costs, leading to competitive disadvantages for traditional pharmacies [20][23]. - The profitability of self-service machines is questioned, as some operators report low revenue compared to the initial investment required for the machines [29][30]. - The potential for self-service machines to take over the market raises concerns about the sustainability of traditional pharmacies, especially in densely populated urban areas where competition is already fierce [34][35].

2024年，亨迪药业实现营业收入4.46亿元，同比下降32.75%；实现归属于上市公司股东的净利润 9154.74万元，同比下降48.02%；实现归属于上市公司股东的扣除非经常性损益的净利润7295.50万元， 同比下降57.14%；经营活动产生的现金流量净额为9607.32万元，同比下降29.91%。 彼时，亨迪药业表示，公司营业收入下降主要源于主产品布洛芬销量减少，国际市场竞争激烈，价格低 位运行，公司调整销售策略以规避低价竞争。这一调整虽属应对市场之举，但对营收规模造成了明显冲 击。 原料药是亨迪药业的重中之重，该板块贡献收入占公司总收入比重长期在80%左右，其中，布洛芬是最 主要的品类。一旦布洛芬原料药产品放量受阻，亨迪药业的业绩表现就会出现较大变动。 亨迪药业的研发费用亦呈下降趋势。2024年、2025年上半年，亨迪药业的研发费用分别为3293.71万 元、1587.62万元，较上年同期分别下降37.59%、17.72%。亨迪药业称，研发投入下降系本期新增制剂 一致性评价项目较上期减少所致。有业内人士指出，研发投入的大幅收缩可能会对公司未来的产品创新 和市场竞争力产生一定影响，长期来看，亨迪药业需平 ...