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Kexing Pharmaceutical's Human Erythropoietin Injection was awarded the "Approval Notice for Supplementary Drug Application"

 Last Update: 2022-03-07
 Source: Internet
 Author: User

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On February 14, Kexing Pharmaceuticals announced that it received the “Approval Notice for Supplementary Drug Application” approved and issued by the State Food and Drug Administration on February 12.

In the treatment of "anemia caused by chemotherapy of non-myeloid malignant tumors", large-scale human erythropoietin products can significantly reduce the frequency of medication, and improve the patient's medication compliance under the premise of equal efficacy

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