Sodium Glycero-phosphate Injection (10 ml: 2.16 g) by Shijiazhuang Sihua Pharmaceutical Group Has Been Approved


发布时间:2025-12-25

【概要描述】 At the year’s end, good news abounds as we sprint toward the completion of our annual R&D objectives and achieve yet another significant milestone! On December 25, Shijiazhuang Sihua Pharmaceutical Group received approval from the National Medical Products Administration for the production registration of its Class 4 chemical drug—sodium glycerophosphate injection (10 mL: 2.16 g)—which is also deemed to have passed the evaluation of quality and therapeutic equivalence for generic drugs, making it the third such product approved in China. This marks the Group’s 93rd newly approved product this year and its 69th new dosage-form product.
At the year’s end, good news abounds as we sprint toward our annual R&D targets and achieve yet another significant milestone! On December 25, Shijiazhuang Sihua Pharmaceutical Group’s Class 4 chemical drug—sodium glycerophosphate injection (10 mL: 2.16 g)—received production registration approval from the National Medical Products Administration, and is deemed to have passed the evaluation of generic drug quality and therapeutic equivalence, making it the third such product approved in China. This marks the group’s 93rd new product approval this year and its 69th new dosage-form product approval.
According to available information, sodium glycerophosphate injection is a nutritional drug that can be used as a phosphorus supplement in parenteral nutrition for adults and in patients with phosphorus deficiency. Data from MeneNet indicate that in 2024, sales of sodium glycerophosphate injection across China’s three major distribution channels—urban public hospitals, county-level public hospitals, and township health centers—totaled approximately RMB 50 million, with first-half 2025 sales reaching about RMB 30 million.
The approval of sodium glycerophosphate injection this time further enriches the Group’s product portfolio in the areas of electrolyte and acid–base balance, as well as mineral and nutritional supplementation. To date, the Group has a total of 166 drug varieties comprising 217 dosage forms that have either passed or are deemed to have passed the bioequivalence and therapeutic equivalence evaluation for generic drugs.
 

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