Group 1 - The company Fangsheng Pharmaceutical announced that its subsidiary GuangDong Fangsheng Ronghua Pharmaceutical Co., Ltd. has received a Drug Production License from the Guangdong Provincial Drug Administration [2] - The license allows the subsidiary to act as the marketing authorization holder for the production of Riluzole tablets, with a validity period until January 26, 2031 [2]

Group 1 - Company Jianhui Information plans to acquire 38% equity in Boke Guoxin for RMB 73.71 million, increasing its stake from 32% to 70%, making Boke Guoxin a subsidiary [1] - Company Guangshengtang's innovative drug GST-HG141 for hepatitis B has completed the enrollment of 578 participants in its Phase III clinical trial [2] - Company Hongjing Optoelectronics is establishing a partnership with a target scale of RMB 290 million, contributing RMB 3 million as a limited partner [3] Group 2 - Company Hongchang Technology intends to acquire 21% equity in Liangzhi Joint, which will make it the controlling shareholder with a 51% stake [4] - Company Xiexin Integrated has not yet received any orders in the "space photovoltaic" sector, which remains in the exploratory phase [5] - Company Xianheng International plans to reduce its shareholding by up to 3%, amounting to a maximum of 12.28 million shares [6] Group 3 - Company Furuijia plans to reduce its repurchased shares by up to 2%, totaling 18.93 million shares [7] - Company Tianqimo is planning to issue shares and pay cash to acquire assets, leading to a temporary suspension of its stock [8] - Company Shuangqiang Technology's director plans to reduce his holdings by up to 0.32% [9] Group 4 - Company Bairun plans to adjust the conversion price of its bonds due to stock prices falling below 85% of the conversion price [11] - Company Dongnan Network has won an EPC project worth RMB 994 million [12] - Company Anhui Energy has appointed Xu Wengong as the new general manager following the resignation of Fang Shiqing [13] Group 5 - Company Lijun plans to invest up to USD 3 million to establish subsidiaries in Hong Kong and Peru [14] - Company Zhenghe Ecology has signed a strategic cooperation agreement with the government of Beijing's Miyun District [15] - Company First Venture has elected Guo Chuan as the chairman of its board [16] Group 6 - Company Changxin Bochuang's shareholder has terminated an agreement to transfer 14.5 million shares [17] - Company Hengrui Medicine's HR091506 tablet application has been accepted by the National Medical Products Administration [18] - Company Hengrui Medicine's SHR-1894 injection has received approval for clinical trials [20] Group 7 - Company Longshen Rongfa has obtained a medical device production license [21] - Company Western Securities reported that its new borrowings exceeded 20% of its net assets [22] - Company Rongfa Nuclear Power's subsidiary has won a project worth RMB 101 million [23] Group 8 - Company Taiji Industry's subsidiary has a pre-bid for the Huahong FAB9B project with a bid amount of RMB 3.778 billion [24] - Company Suzhou High-tech plans to increase its investment in a subsidiary by RMB 780 million through a debt-to-equity swap [26] - Company Electric Power Investment's vice president has resigned due to work changes [27] Group 9 - Company Hengwei Technology reported a 30.13% increase in net profit for 2025 [28] - Company Fangsheng Pharmaceutical's subsidiary has received a drug production license [29] - Company Pilin Bio's subsidiary has received a notice for clinical trial acceptance for a hemostatic drug [31] Group 10 - Company Zhongxin Fluorine Material has received approval for a stock issuance to specific investors [32] - Company Shanhe Intelligent expects a total transaction amount with related parties to be RMB 1.197 billion in 2026 [33] - Company Warner Pharmaceutical's partner has completed Phase I clinical trials for a new drug [34]

Core Viewpoint - Fangsheng Pharmaceutical (603998.SH) has received a Drug Production License from the Guangdong Provincial Drug Administration for its subsidiary, Guangdong Fangsheng Ronghua Pharmaceutical Co., Ltd., allowing it to act as the marketing authorization holder for RuLuGuoLi tablets [1] Group 1 - The acquisition of the Drug Production License will help the company and its subsidiary integrate and allocate production and sales resources [1] - This license is expected to improve capacity utilization and reduce production costs for the company [1] - The short-term impact on the company's performance is not expected to be significant following the receipt of the Drug Production License [1]

湖南方盛制药股份有限公司 HUNANFANGSHENG PHARMACEUTICAL CO., LTD. 证券代码：603998 证券简称：方盛制药 公告编号：2026-009 湖南方盛制药股份有限公司 关于控股子公司获得《药品生产许可证》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法律责任。 近日，湖南方盛制药股份有限公司（以下简称"公司"或"方 盛制药"）控股子公司广东方盛融华药业有限公司（以下简称"方 盛融华"）收到广东省药品监督管理局颁发的《药品生产许可证》， 同意方盛融华作为药品上市许可持有人，方盛制药作为受托方, 受托产品为瑞卢戈利片。具体情况如下： 一、《药品生产许可证》基本情况 企业名称：广东方盛融华药业有限公司 分类码：Bh 法定代表人：方传龙 企业负责人：欧阳 质量负责人：罗积安 有效期至：2031年1月26日 生产地址和生产范围： 受托方是湖南方盛制药股份有限公司，生产地址是：湖南省 长沙市麓松路 789 号，受托产品为瑞卢戈利片（仅限上市注册）。 二、对上市公司的影响及风险提示 社会信用代码：91440 ...

Core Viewpoint - Fangsheng Pharmaceutical (603998.SH) has received a Drug Production License from the Guangdong Provincial Drug Administration for its subsidiary, Guangdong Fangsheng Ronghua Pharmaceutical Co., Ltd., allowing it to act as the marketing authorization holder for RuLuGuoLi tablets [1] Group 1 - The acquisition of the Drug Production License will help the company and its subsidiary integrate and allocate production and sales resources [1] - This license is expected to improve capacity utilization and reduce production costs for the company [1] - The short-term impact on the company's performance is not expected to be significant following this license acquisition [1]

Core Viewpoint - Fangsheng Pharmaceutical (603998.SH) has received a Drug Production License from the Guangdong Provincial Drug Administration for its subsidiary, Guangdong Fangsheng Ronghua Pharmaceutical Co., Ltd., allowing it to hold the marketing authorization for RuLuGuoLi tablets [1] Group 1 - The Drug Production License enables the company and its subsidiary to integrate and allocate production and sales resources [1] - This development is expected to improve capacity utilization and reduce production costs [1] - The immediate impact on the company's financial performance is not expected to be significant [1]

Core Viewpoint - Fangsheng Pharmaceutical's subsidiary, Guangdong Fangsheng Ronghua Pharmaceutical Co., Ltd., has received a Drug Production License from the Guangdong Provincial Drug Administration, allowing it to act as the marketing authorization holder for the drug Riluzole Tablets, with Fangsheng Pharmaceutical as the entrusted party [1] Group 1 - The approval of the Drug Production License signifies a key regulatory milestone for Fangsheng Ronghua, enhancing its operational capabilities in the pharmaceutical market [1] - Riluzole Tablets are indicated for the treatment of amyotrophic lateral sclerosis (ALS), which may expand the company's product portfolio and market reach [1] - The collaboration between Fangsheng Ronghua and Fangsheng Pharmaceutical indicates a strategic partnership aimed at leveraging each other's strengths in drug development and commercialization [1]

Core Viewpoint - The Chinese medicine industry is currently facing significant challenges, including regulatory changes that may lead to the elimination of many traditional Chinese medicine products, but this could also serve as an opportunity for industry upgrade and quality improvement [7][9][33]. Group 1: Industry Performance and Market Sentiment - After the "924" market trend in 2024, the Shenwan Chinese Medicine Index has been adjusted and has continued to consolidate, with a cumulative decline of over 10% [3]. - Even with performance forecasts indicating profit growth for Chinese medicine companies, the market has not responded positively, as seen with WoHua Pharmaceutical's net profit doubling yet experiencing a 6.01% drop in stock price the following day [4]. - The recent negative sentiment in the market is largely due to the impending withdrawal of a large number of traditional Chinese medicine products, as new regulations require clearer safety information on product labels [7][8]. Group 2: Regulatory Changes and Industry Impact - The new regulations state that any traditional Chinese medicine product with unclear safety information will not be approved for re-registration after July 1, 2026, affecting approximately 57,000 existing products, with over 70% facing safety information issues [7]. - The industry is experiencing a "compliance storm," which is seen not merely as a phase of elimination but as a catalyst for quality improvement and modernization of traditional Chinese medicine [9][11][33]. Group 3: Strategies for Development - To survive, companies must focus on supplementing safety data and revising product labels to ensure compliance with new regulations [15][16]. - Many leading companies have already completed the revision of their core products' labels, indicating a proactive approach to compliance [19]. - The compliance costs associated with these changes are manageable for companies with market support, as evidenced by several firms maintaining profitability despite the regulatory pressures [22][24]. Group 4: Innovation and Future Growth - Beyond compliance, companies need to invest in innovative research and development to ensure long-term growth, especially in a challenging market environment characterized by price reductions and weak consumer demand [27]. - New drug classifications in traditional Chinese medicine include ancient classic formulas, improved formulations, and innovative drugs, with the latter representing the highest potential for future competitiveness [28][30]. - Companies like Kangyuan Pharmaceutical and Shenwei Pharmaceutical are leading in innovation, having received multiple approvals for new products, indicating a focus on future growth opportunities [30][31].

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法律责任。 ● 重要内容提示： 登录新浪财经APP 搜索【信披】查看更多考评等级 证券代码：603998 证券简称：方盛制药 公告编号：2026-008 湖南方盛制药股份有限公司 关于公司参与投资设立的并购基金对外出售投资 项目部分股份的进展公告 1、同系方盛已于近期召开合伙人会议，同意将其存续期延长一年至2027年1月31日，同意同系泰兴、同 系未来将其分别持有的同系方盛未实缴出资额31.70万元（实缴出资28.30万元）、285.30万元退伙（实 缴出资254.70万元），同系方盛认缴出资额由47,065.83万元减少为46,748.83万元； 2、根据此前约定，同系方盛在收回全部回购款项后不再持有湖南珂信股权；此外，目前武汉珂信6%的 股权已过户至同系方盛名下； 3、根据湖南珂信提供的长沙珂信相关数据，长沙珂信2025年度扣除非经常性损益后的净利润已达到向 盈康生命作出的首年业绩承诺目标，预计将触发盈康生命收购湖南珂信持有的长沙珂信29%股权的条 件，但具体交易尚需要各方履行相关审批程 ...

Core Viewpoint - Fangsheng Pharmaceutical (603998) emphasizes its focus on innovative traditional Chinese medicine (TCM) and classic TCM products, highlighting their clinical value and adherence to regulatory standards [1] Product Overview - The company’s main products include innovative TCM such as Xiaoer Jingxing Zhike Granules, Xuanqi Jianguo Tablets, and Yangxue Qufeng Zhitong Granules, all of which have undergone Phase II and III clinical trials [1] - Innovative TCM products are based on TCM theory and clinical practice, featuring breakthroughs in formulation, process, and standards, with strict quality control and minimal side effects due to their natural origins [1] - Classic TCM products include Tenghuang Jianguo Tablets, Xuesaitong Tablets/Dispersible Tablets, and Qiangli Pipa Syrup (Honey-Processed)/Liquid, which have completed or are in the process of revising safety content in their instructions [1] Regulatory Compliance - The company is attentive to regulatory policy adjustments in the TCM industry and prioritizes the safety and efficacy of its products, ensuring compliance with national drug regulatory requirements in its production and R&D activities [1]