Quickly check!These 17 batches of medicines do not meet the regulations!Sale and recall

On the 15th, the State Drug Administration issued a notice on 17 batches of medicines that did not meet the requirements:

After inspection by the Hubei Provincial Institute of Drug Administration, the two batches of acetylcysteine ​​injection produced by Shanxi Guorun Pharmaceutical Co., Ltd. did not meet the regulations and did not meet the specified projects as hydrogen sulfide.

After inspection by the Jiangxi Provincial Academy of Pharmaceutical Inspection and Inspection, the two batches of Huoxiang Zhengqi water produced by Hubei Tongdutang Pharmaceutical Co., Ltd. did not meet the requirements, and did not meet the requirements of the regulations.

After inspection by the China Food and Drug Inspection Research Institute, it is marked as Hebei Anguo Zhenyu Pharmaceutical Co., Ltd., Shanghai Wanshi Cheng Pharmaceutical Co., Ltd., Shaoxing Zhenyuan Traditional Chinese Medicine Drinking Co., Ltd., Anhui Tongtai Zutang Pharmaceutical Co., Ltd. Shenghai Traditional Chinese Medicine Drinking Co., Ltd., Jiangxi Zhongkang Traditional Chinese Medicine Drinking Co., Ltd., Guangdong Shizhe Pharmaceutical Co., Ltd. and Gansu Guogao Pharmaceutical Co., Ltd. did not meet the regulations, and the project was not in line with the regulations to disable pesticide residues.

After inspection by the Gansu Provincial Academy of Pharmaceutical Inspection and Research, a batch of Qiancao produced by Sichuan Yuancao Traditional Chinese Medicine Drinking Co., Ltd. did not meet the requirements, and did not meet the specified projects including traits and identification.

After inspection by the China Food and Drug Inspection Research Institute, it is marked that 4 batches of authentic purple grass produced by Hebei Honghan Pharmaceutical Co., Ltd., Xinjiang Enze Traditional Chinese Medicine Drinking Co., Ltd. and Huayi Huayi Traditional Chinese Medicine Drinking Factory Co., Ltd. It meets the specified projects as traits.

For the above -mentioned do not meet the prescribed drugs, the drug supervision and management department has required relevant enterprises and units to take risk control measures such as suspension of sales and use, recall, and conducting investigations and rectification on reasons that do not meet the prescribed reasons.

The State Drug Administration requires relevant provincial drug supervision and management departments to organize investigations on suspected illegal acts existing above -mentioned enterprises and units in accordance with the Drug Administration Law of the People's Republic of China, and publicize the results of the results in accordance with regulations.

Source: National Drug Administration

Edit: Wang Jing

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