Good News! A New Specification of Compound Potassium Dihydrogen Phosphate Injection (2 ml) from Shijiazhuang Sihua Pharmaceutical Group Has Been Approved.


发布时间:2026-01-27

【概要描述】 A new year ushers in a fresh start, with innovation never pausing. On January 26, the supplemental application for the Class 3 chemical drug—potassium hydrogen phosphate injection (2 ml)—developed by Shijiazhuang Sihua Pharmaceutical Group was approved by the National Medical Products Administration and is deemed to have passed the consistency evaluation. This product marks another newly approved dosage form for the Group, following the approval of the potassium hydrogen phosphate injection (5 ml) in January 2025, and represents the second new product the Group has secured since the beginning of this year.
A new year ushers in a fresh start, with innovation never pausing. On January 26, the supplemental application for the Class 3 chemical drug—potassium hydrogen phosphate injection (2 ml)—developed by Shijiazhuang Sihua Pharmaceutical Group was approved by the National Medical Products Administration and is deemed to have passed the consistency evaluation. This product marks another newly approved dosage form following the approval in January 2025 of the potassium hydrogen phosphate injection (5 ml), and it is also the second new product the group has secured approval for since the beginning of this year.
According to available information, potassium hydrogen phosphate compound injection is an inorganic phosphate supplement. This product is primarily used as a phosphate supplement in total parenteral nutrition, such as in patients undergoing moderate-to-severe surgery or other traumatic injuries who require fasting for more than five days; it may also be employed in the management of hypophosphatemia secondary to certain diseases.
The approval of this specification and product variety further enriches the Group’s product pipeline and portfolio, while providing more treatment options for adult and pediatric patients with hypophosphatemia and those receiving parenteral nutrition. To date, the Group has a total of 167 products across 219 dosage forms that have either passed or are deemed to have passed the Consistency Evaluation for Quality and Therapeutic Equivalence of Generic Drugs.
 

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