北京中关村科技发展(控股)股份有限公司关于下属公司北京华素盐酸纳曲酮片通过一致性评价的公告

Core Viewpoint - Beijing Zhongguancun Science and Technology Development (Holding) Co., Ltd. announced that its subsidiary, Beijing Huasu Pharmaceutical Co., Ltd., has successfully passed the consistency evaluation for the drug "Naltrexone Hydrochloride Tablets" [1][2] Group 1: Drug Approval and Details - The drug "Naltrexone Hydrochloride Tablets" (specification: 50mg) has received approval from the National Medical Products Administration, confirming its quality and efficacy consistency evaluation [1][2] - The original manufacturer of Naltrexone is TEVA WOMENS, which received approval in the United States in 1984 under the brand name REVIA [2] - Currently, there are no original or imported generic versions of this drug available in China, making Beijing Huasu the sole provider of this product in the market [2] Group 2: Financial and R&D Investment - The total research and development investment for the consistency evaluation project of Naltrexone Hydrochloride Tablets has reached 11.7389 million yuan [3] Group 3: Market Impact and Competitive Advantage - The approval of the consistency evaluation is expected to enhance the company's market competitiveness and positively impact its operating performance [4] - The drug will receive support in terms of medical insurance payments, and medical institutions are encouraged to prioritize its procurement and clinical use [4] - The successful evaluation provides valuable experience for the company in conducting future consistency evaluations for other generic drugs [4]