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花园生物(300401.SZ):花园药业收到硫辛酸片、比索洛尔氨氯地平片的药品注册证书
Ge Long Hui A P P· 2025-08-25 08:19
Core Viewpoint - Garden Biologics (300401.SZ) announced that its wholly-owned subsidiary, Zhejiang Garden Pharmaceutical Co., Ltd., has received the drug registration certificates for "Alpha-Lipoic Acid Tablets" and "Bisoprolol Amlodipine Tablets" from the National Medical Products Administration [1] Group 1 - The "Alpha-Lipoic Acid Tablets" are primarily used for the treatment of diabetic peripheral neuropathy [1] - The "Bisoprolol Amlodipine Tablets" are mainly used for the treatment of hypertension and can be used alone or in combination with other antihypertensive medications [1]
花园生物:子公司取得药品注册证书
Xin Lang Cai Jing· 2025-08-25 08:18
Core Viewpoint - The company has received drug registration certificates for "Alpha-Lipoic Acid Tablets" and "Bisoprolol Amlodipine Tablets" from the National Medical Products Administration, which will enhance its product line and positively impact its development [1] Group 1 - The full subsidiary Zhejiang Huayuan Pharmaceutical Co., Ltd. has been approved for the registration of "Alpha-Lipoic Acid Tablets," which are primarily used for treating diabetic peripheral neuropathy [1] - The "Bisoprolol Amlodipine Tablets" are mainly used for the treatment of hypertension [1] - Obtaining these drug registration certificates will further enrich the company's product line and promote the upgrade of product capabilities [1]
福安药业:子公司收到硫辛酸片药品注册证书
news flash· 2025-07-21 08:48
Core Insights - Fuan Pharmaceutical's wholly-owned subsidiary, Yantai Zhichu Pharmaceutical Co., Ltd., has received a drug registration certificate for Alpha-Lipoic Acid Tablets from the National Medical Products Administration [1] - The drug is classified as a Class 3 chemical drug and is available in specifications of 0.2g and 0.6g [1] - The indication for Alpha-Lipoic Acid Tablets is for the treatment of sensory abnormalities caused by diabetic peripheral neuropathy [1] - A total of four companies, including Zhichu Pharmaceutical, have either passed or are deemed to have passed the consistency evaluation for this drug [1]