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In order to further protect the safety of public medication, the State Drug Administration has decided to revise the instructions for systemic fluoroquinolones
1.
If the revised content involves the label of a drug, it shall be revised together; the instructions and other content of the label shall be consistent with the original approved content
2.
3.
4.
5.
Hereby announce
Attachment: Requirements for the revision of the package insert of fluoroquinolones for systemic use
State Food and Drug Administration
March 18, 2021
Annex to Announcement No.