Shijiazhuang Sihua Pharmaceutical Group’s Pentoxifylline Injection and Ipratropium Bromide Solution for Inhalation Have Been Approved
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发布时间:2022-10-11
【概要描述】
Recently, two products—pentoxifylline injection (5 mL: 0.1 g) and ipratropium bromide solution for inhalation (2 mL: 0.5 mg and 2 mL: 0.25 mg)—developed by Shijiazhuang Sihua Pharmaceutical Group, each available in three specifications, were simultaneously granted drug registration certificates by the National Medical Products Administration. These products are also deemed to have passed the evaluation of quality and therapeutic equivalence for generic drugs, with pentoxifylline injection (5 mL: 0.1 g) becoming the first such product from a domestic pharmaceutical company to receive this designation.
In the golden autumn season, Shijiazhuang No.4 Pharmaceutical has reaped abundant achievements in scientific research and innovation. Recently, two products—pentoxifylline injection (5 mL: 0.1 g) and ipratropium bromide solution for inhalation (2 mL: 0.5 mg and 2 mL: 0.25 mg)—developed by Shijiazhuang No.4 Pharmaceutical Group, each available in three specifications, were simultaneously granted drug registration certificates by the National Medical Products Administration. These products are also deemed to have passed the evaluation of quality and therapeutic equivalence for generic drugs, with pentoxifylline injection (5 mL: 0.1 g) becoming the first such product from a domestic pharmaceutical company to receive this designation.
According to reports, pentoxifylline injection is primarily used to treat peripheral arterial disease and inner-ear circulatory disorders, while ipratropium bromide solution for inhalation is mainly indicated for the relief of bronchospasm associated with chronic obstructive pulmonary disease, including chronic bronchitis, emphysema, and asthma.
In recent years, Shijiazhuang Sihua Pharmaceutical Group has increasingly demonstrated its innovative strengths. Since the beginning of this year, the company has obtained 35 product approvals, including 26 for finished dosage forms. To date, a total of 31 drug varieties encompassing 41 specifications have either passed or been deemed to have passed the National Evaluation of Quality and Therapeutic Equivalence for Generic Drugs. The group’s efficiency and volume of specialized generic drug R&D rank among the top in the national pharmaceutical industry, with innovation effectively driving the continuous optimization and upgrading of the company’s product portfolio and value chain.
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