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Announcement of the State Food and Drug Administration on the conversion of Guifu Dihuang Granules into over-the-counter drugs (No. 52 of 2021)

 Last Update: 2021-07-08
 Source: Internet
 Author: User

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According to the "Administrative Measures for the Classification of Prescription Drugs and Over-the-Counter Drugs (Trial)" (formerly State Drug Administration Order No.

Before July 6, 2021, the holder of the relevant drug marketing authorization shall submit a supplementary application for the revision of the drug label in accordance with the "Administrative Measures on Drug Registration" and other relevant regulations, and submit it to the provincial drug regulatory authority for record, and promptly notify the relevant contents of the revision of the label Medical institutions, pharmaceutical companies and other units

The contents of the non-prescription drug inserts other than those specified in the template inserts shall be implemented in accordance with the original approval documents

Hereby announce

Attachment: 1.

State Food and Drug Administration

April 7, 2021

Announcement No.

Annex 2 of the Announcement No.

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