Valsartan/Amlodipine Tablets (I) of Shijiazhuang Sihua Pharmaceutical Group Approved
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发布时间:2022-09-26
【概要描述】
Recently, Shijiazhuang Sihua Pharmaceutical Group announced another significant achievement in its research and development efforts: the Class 4 chemical drug valsartan amlodipine tablets (I), developed by the company, has been granted a Drug Registration Certificate by the National Medical Products Administration and is deemed to have passed the evaluation of quality and therapeutic equivalence for generic drugs.
Recently, Shijiazhuang Sihua Pharmaceutical Group announced another significant achievement in its research and development efforts: the Class 4 chemical drug valsartan amlodipine tablets (I), developed by the company, has been granted a Drug Registration Certificate by the National Medical Products Administration and is deemed to have passed the evaluation of quality and therapeutic equivalence for generic drugs.
According to reports, Valsartan/Amlodipine Tablets (I) are primarily indicated for the treatment of essential hypertension and for patients whose blood pressure is not adequately controlled with monotherapy. Hypertension is a common chronic disease, and Valsartan/Amlodipine Tablets (I) is the only single-tablet combination antihypertensive agent included in the National Essential Medicines List; it is also the first compound solid dosage form developed by Shijiazhuang Sihua Pharmaceutical to receive regulatory approval. Single-tablet combination formulations have emerged as a new trend in the management of hypertension due to their ability to reduce the number of pills patients need to take, enhance convenience of use, and improve treatment adherence and efficacy.
In recent years, Shijiazhuang Sihua Pharmaceutical has accumulated substantial R&D achievements, which have provided strong momentum for the company’s competitive development and continuously elevated its industrial chain toward the high end of the value chain. Since the beginning of this year, the company has obtained 30 product approvals, including 20 formulation approvals, placing it at the forefront of the industry in terms of approval volume.
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