Core Viewpoint - The company has received approval from the National Medical Products Administration for the registration of aluminum magnesium carbonate chewable tablets, which enhances its product pipeline and supports sustainable development [1][4]. Drug Basic Information - Drug Name: Aluminum Magnesium Carbonate Chewable Tablets - Dosage Form: Tablet - Specification: 0.5g - Registration Classification: Class 4 Chemical Drug - Approval Number: Guo Yao Zhun Zi H20263134 - License Holder: Hunan Qianjin Xiangjiang Pharmaceutical Co., Ltd. - Approval Conclusion: The drug meets registration requirements and is classified as a Class A over-the-counter medication [1]. Drug Efficacy and Market Potential - Aluminum magnesium carbonate chewable tablets are a first-line medication for the digestive system, providing antacid, bile acid neutralization, and mucosal protection, suitable for treating various gastric diseases including acute and chronic gastritis, gastric and duodenal ulcers, and gastroesophageal reflux disease [2]. - The product is projected to have a total sales volume of 990 million yuan in the domestic medical and retail markets by 2024 [2]. R&D Investment - As of the announcement date, the cumulative R&D investment in aluminum magnesium carbonate chewable tablets by Qianjin Xiangjiang Pharmaceutical is 1.0047 million yuan [3]. Impact on the Company - The approval of aluminum magnesium carbonate chewable tablets is seen as a significant step in enhancing the company's product offerings, contributing positively to its sustainable growth [4].
株洲千金药业股份有限公司 关于子公司获得药品注册证书的公告