Good News in the Golden Autumn! Shijiazhuang Sihua Pharmaceutical Group’s Linezolid Sodium Chloride Injection (300 ml) Has Been Approved


发布时间:2023-10-17

【概要描述】 In the golden autumn season, Shijiazhuang No. 4 Pharmaceutical has reaped a series of breakthroughs in research and development innovation. On October 17, the group’s linezolid sodium chloride injection (300 ml), submitted as a Class 3 chemical drug, received approval for drug production registration from the National Medical Products Administration and is deemed to have passed the consistency evaluation. This follows the group’s earlier receipt, within the past week, of production registration approvals for tinidazole tablets (0.5 g) and ornidazole tablets (0.5 g), marking yet another new product approval.
In the golden autumn season, Shijiazhuang No. 4 Pharmaceutical has reaped a series of breakthroughs in R&D and innovation. On October 17, the company’s linezolid sodium chloride injection (300 ml), submitted as a Class 3 chemical drug, received approval for drug production registration from the National Medical Products Administration, which also deems it to have passed the consistency evaluation. This follows closely on the heels of the company’s earlier receipt, within the past week, of production registration approvals for tinidazole tablets (0.5 g) and ornidazole tablets (0.5 g), marking yet another new product approval for Shijiazhuang No. 4 Pharmaceutical.
According to reports, linezolid sodium chloride injection is indicated for the treatment of infections caused by susceptible strains of specific microorganisms, including hospital-acquired pneumonia, community-acquired pneumonia, complicated skin and soft-tissue infections, and uncomplicated skin and soft-tissue infections.
Previously, the Group obtained marketing approval for Linezolid Glucose Injection (100 mL) in 2021. The recent approval of this new product further enriches the Group’s product pipeline and enhances its market competitiveness. To date, the Group has either obtained or been deemed to have obtained consistency evaluation for a total of 59 drug varieties encompassing 77 dosage forms.

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