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亿帆医药:公司始终专注于主营业务发展
Zheng Quan Ri Bao Wang· 2025-10-24 09:13
Core Viewpoint - Yifan Pharmaceutical (002019) remains focused on its core business development and reports that operations are running smoothly, with management expressing confidence in future growth [1] Company Summary - The company is actively engaging with investors through interactive platforms, indicating a commitment to transparency and communication [1] - Management's confidence suggests a positive outlook for the company's strategic direction and operational performance [1]
亿帆医药:公司最近暂无机构投资者现场调研活动
Mei Ri Jing Ji Xin Wen· 2025-10-22 01:31
Core Viewpoint - Recently, there have been no on-site research activities conducted by institutional investors for Yifan Pharmaceutical (002019.SZ) [1] Company Summary - Yifan Pharmaceutical confirmed on October 22 that there have been no recent on-site research activities by institutional investors [1]
亿帆医药:目前还没有收到合作方对F627销售情况的反馈
Mei Ri Jing Ji Xin Wen· 2025-10-17 08:19
Core Viewpoint - The company has not yet received feedback from its exclusive U.S. distributor regarding the sales performance of F627 in the third quarter [1] Group 1 - An investor inquired about the sales situation of F627 in the U.S. and whether it met or exceeded expectations [1] - The company expressed gratitude for the inquiry and confirmed the lack of feedback from its partner [1]
亿帆医药涨2.12%,成交额5379.66万元,主力资金净流入507.23万元
Xin Lang Cai Jing· 2025-10-15 02:29
Core Viewpoint - Yifan Pharmaceutical's stock has shown a year-to-date increase of 31.64%, with recent fluctuations indicating a slight decline over the past 20 and 60 days, suggesting potential volatility in the near term [1][2]. Financial Performance - For the first half of 2025, Yifan Pharmaceutical reported a revenue of 2.635 billion yuan, reflecting a year-on-year growth of 0.11%, while the net profit attributable to shareholders was 304 million yuan, marking a significant increase of 19.91% [2]. - Cumulatively, since its A-share listing, Yifan Pharmaceutical has distributed a total of 1.328 billion yuan in dividends, with 243 million yuan distributed over the past three years [3]. Shareholder Information - As of September 30, 2025, the number of shareholders for Yifan Pharmaceutical stood at 46,600, a decrease of 0.46% from the previous period, while the average number of circulating shares per person increased by 0.46% to 18,048 shares [2]. - The second-largest circulating shareholder is Hong Kong Central Clearing Limited, holding 25.5819 million shares, which is an increase of 2.4783 million shares compared to the previous period [3]. Stock Performance - As of October 15, Yifan Pharmaceutical's stock price was 13.98 yuan per share, with a trading volume of 53.7966 million yuan and a turnover rate of 0.46%, resulting in a total market capitalization of 17.005 billion yuan [1]. - The stock has experienced a net inflow of main funds amounting to 5.0723 million yuan, with significant buying and selling activity from large orders [1].
方盛制药:受让“复方醋酸地塞米松乳膏”药品上市许可
Xin Lang Cai Jing· 2025-10-09 08:00
Core Viewpoint - The transaction between Fangsheng Pharmaceutical and Yifan Pharmaceutical involves the acquisition of the marketing authorization for "Compound Dexamethasone Acetate Cream," which is expected to enhance the company's product portfolio in dermatology and potentially serve as a new profit growth point [1] Group 1: Transaction Details - The contract was signed on September 30, 2025, and does not constitute a related party transaction or a major asset restructuring, falling within the chairman's approval authority [1] - The payment for the transaction will be made in three phases, indicating a structured financial approach to the acquisition [1] Group 2: Market Context - The drug is used for various skin diseases, with 103 companies in China holding production licenses for it [1] - In the first half of 2025, the sales revenue from physical pharmacies for this drug reached 175 million yuan, highlighting its market potential [1] Group 3: Strategic Implications - The acquisition aligns with the company's development strategy to expand its dermatological product offerings, which is expected to contribute positively to future revenue streams [1] - However, the timeline for completing the holder change procedures remains uncertain, and sales may be influenced by market factors, necessitating cautious decision-making by investors [1]
亿帆医药股份有限公司关于全资子公司收到药品注册受理通知书的公告
Core Points - Yifan Pharmaceutical's subsidiary Sichuan Defeng Pharmaceutical has received a drug registration acceptance notice from the National Medical Products Administration for the production of Sodium Sapropterin Dihydrochloride Powder [1][2] - The drug is intended for patients with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin (BH4) responsive phenylketonuria (PKU) and is applicable for adults and children over one month old [1][2] - The company has invested approximately 4.22 million yuan in the research and development of this project [4] Drug Registration Details - Acceptance Number: CYHS2503557 - Drug Name: Sodium Sapropterin Dihydrochloride Powder - Application Type: Domestic production drug registration license - Specification: 100mg (calculated as C9H15N5O3·2HCl) - Drug Registration Category: Class 3 chemical drug - Applicant: Sichuan Defeng Pharmaceutical [1][2] Market Context - As of the report date, Yifan Pharmaceutical is the only company in China to apply for the registration of Sodium Sapropterin Dihydrochloride Powder, with only one other company, Annora Pharma Private Limited, having submitted a registration for a different category [2] - There are currently no Sodium Sapropterin Dihydrochloride Powder products available on the domestic market [2] - According to IQVIA, the global sales for Sodium Sapropterin Dihydrochloride Powder are projected to be approximately 100 million USD in 2024 [3]
亿帆医药:关于全资子公司收到药品注册受理通知书的公告
Zheng Quan Ri Bao· 2025-09-29 11:49
Core Viewpoint - Yifan Pharmaceutical announced that its wholly-owned subsidiary, Sichuan Defeng Pharmaceutical Co., Ltd., has received the acceptance notice for the domestic production registration application of Salbutamol Sulfate Powder from the National Medical Products Administration [2] Group 1 - The acceptance notice indicates a significant step towards the commercialization of Salbutamol Sulfate Powder, which may enhance the company's product portfolio [2] - The approval process reflects the regulatory compliance and potential market entry for the new pharmaceutical product [2]
9月29日晚间重要公告一览
Xi Niu Cai Jing· 2025-09-29 10:45
Group 1 - Yinglian Co., Ltd. expects a net profit increase of 1531.13% to 1672.97% year-on-year for the first three quarters of 2025, with projected revenue of 1.63 billion to 1.65 billion yuan, a growth of 9.49% to 10.83% [1] - Meixin Sheng plans to reduce its shareholding by no more than 1% through centralized bidding and block trading [1] - Huayin Technology signed two sales contracts totaling 402 million yuan, with one contract for special functional materials and another for research project materials [3] Group 2 - Shen Highways reported a total toll revenue of 114 million yuan for August [5] - Dash Smart signed a contract worth 113 million yuan for a smart hospital project [7] - Tianbang Food received an administrative regulatory measure decision from the China Securities Regulatory Commission for failing to disclose information in a timely manner [8] Group 3 - Fashilong plans to invest 250 million yuan to establish a wholly-owned subsidiary focused on AI applications and cloud computing [10] - Junpu Intelligent received a government subsidy of 20 million yuan, accounting for 243.97% of its audited net profit for 2024 [11] - Longyun Co. plans to apply for a bank credit limit of 32 million yuan [12] Group 4 - Yifan Pharmaceutical's subsidiary received acceptance for a drug registration application for a medication used to lower phenylalanine levels in patients [12] - Rundu Co. received a drug registration certificate for a hypertension medication [13] - Huahai Qingke elected a new employee director and appointed a new vice president [17] Group 5 - Wanyi Technology received a government subsidy of 173,000 yuan [19] - Haizheng Pharmaceutical's tacrolimus capsules passed the consistency evaluation for generic drugs [20] - Pulaike's new veterinary vaccine received registration certification [22] Group 6 - Boguang New Materials signed a major sales contract estimated at 4.3 billion to 5 billion yuan for nickel powder products [41] - Electric Soul Network announced plans for shareholders to reduce their holdings by up to 1.63% [42] - Jin Haitong's shareholders plan to reduce their holdings by up to 3% [44]
亿帆医药(002019.SZ):盐酸沙丙蝶呤散剂收到药品注册受理通知书
Ge Long Hui A P P· 2025-09-29 08:25
Core Viewpoint - Yifan Pharmaceutical (002019.SZ) has received a production registration acceptance notice from the National Medical Products Administration for its hydrochloride sapropterin dihydrochloride granules, indicating progress in its product development pipeline [1] Group 1: Company Developments - Yifan Pharmaceutical's wholly-owned subsidiary, Sichuan Defeng Pharmaceutical Co., Ltd., has recently received the acceptance notice for the production registration of sapropterin hydrochloride granules [1] - The product is intended for patients with hyperphenylalaninemia (HPA) caused by tetrahydrobiopterin (BH4) responsive phenylketonuria (PKU), applicable for adults and children over one month old [1]
亿帆医药:盐酸沙丙蝶呤散剂药品注册申请获受理
Zhi Tong Cai Jing· 2025-09-29 08:22
Core Viewpoint - Yifan Pharmaceutical (002019.SZ) has received a production registration application acceptance notice from the National Medical Products Administration for its product, Sodium Sapropterin Dihydrochloride Granules, which is intended to treat high phenylalanine levels in patients with phenylketonuria (PKU) [1] Group 1 - Yifan Pharmaceutical's wholly-owned subsidiary, Sichuan Defeng Pharmaceutical Co., Ltd., has recently received the acceptance notice for the production registration application [1] - The product is designed to lower blood phenylalanine (Phe) levels in patients with tetrahydrobiopterin (BH4) responsive phenylketonuria (PKU) [1] - The medication is applicable for adults and children over one month old [1] Group 2 - The company submitted the production registration application to the National Medical Products Administration in September 2025 and received acceptance in the same month [1]