It is forbidden to buy Shuanghuanglian oral preparation modification manual after rush buying

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 It is forbidden to buy Shuanghuanglian oral preparation modification manual after rush buying


The State Food and drug administration requires all relevant production enterprises to report to the provincial drug regulatory authorities for filing before June 30, 2020 according to the revision requirements of the corresponding instructions, and conduct in-depth research on the mechanism of new adverse reactions, take effective measures to do a good job in the publicity and training of drug use and safety issues, and guide doctors and patients to use drugs reasonably.

The reporter of the Beijing News inquired through the database of the State Food and Drug Administration with Shuanghuanglian as the key word. There are 85 approvals, 56 of which belong to oral preparations. Among them, Shuanghuanglian oral liquid is the most, with 13 approvals, which are respectively produced by 12 enterprises such as Sanjing Pharmaceutical Co., Ltd. and Tailong Pharmaceutical Co., Ltd.

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