醋酸氯己定软胶囊

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回盛生物(300871.SZ):醋酸氯己定软胶囊获得新兽药注册证书
Ge Long Hui A P P· 2025-08-27 10:42
Core Viewpoint - The approval of "Chlorhexidine Acetate Soft Capsules" as a new veterinary drug by the Ministry of Agriculture and Rural Affairs of the People's Republic of China marks a significant development for the company and the veterinary pharmaceutical industry [1] Company Summary - Wuhan Huisheng Biotechnology Co., Ltd. and its subsidiaries jointly applied for the new veterinary drug registration [1] - The new veterinary drug registration certificate was issued on August 26, 2025, under the announcement No. 943 by the Ministry of Agriculture and Rural Affairs [1] Industry Summary - The approved drug, Chlorhexidine Acetate Soft Capsules, is intended for use as a disinfectant and antiseptic [1] - It is specifically used to treat vaginal inflammation in pigs caused by sensitive bacteria, prevent postpartum uterine infections, and address endometritis caused by sensitive bacteria [1]
回盛生物:醋酸氯己定软胶囊获得新兽药注册证书
Ge Long Hui· 2025-08-27 10:28
Core Viewpoint - The approval of "Chlorhexidine Acetate Soft Capsules" as a new veterinary drug by the Ministry of Agriculture and Rural Affairs of the People's Republic of China marks a significant development for the company and the veterinary pharmaceutical industry [1]. Company Summary - Wuhan Huisheng Biotechnology Co., Ltd. and its subsidiaries have jointly applied for the new veterinary drug, which has now received official registration [1]. - The new veterinary drug is aimed at treating conditions in pigs, specifically vaginitis caused by sensitive bacteria, and preventing postpartum uterine infections and endometritis [1]. Industry Summary - The approval of new veterinary drugs like Chlorhexidine Acetate Soft Capsules reflects ongoing advancements in the veterinary pharmaceutical sector, enhancing treatment options for livestock [1]. - The regulatory framework under which the drug was approved includes the "Veterinary Drug Management Regulations" and the "Veterinary Drug Registration Measures," indicating a structured approach to drug approval in the industry [1].