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4 enterprise production 5 batches of unqualified drugs By the investigation
 
Author:中国铭铉 企划部  Release Time:2017-4-7 10:05:35  Number Browse:546
 
Medical network on April 7 - April 6, the CFDA website "about 5 batch drug unqualified notice no. 53 (2017), according to the four drug inspection institutions such as jilin pharmaceutical inspection examines, labeled JiLinJi state pharmaceutical co., LTD. Four companies such as the production of 5 batch unqualified drugs. 
 
Unqualified product labeling production enterprises, drug name and batch number is: tianjin da Wan Gong RenTang Beijing pharmaceutical co., LTD., production batch number for 408513 of rheumatism fluid, JiLinJi state pharmaceutical co., LTD., production batch number is 20160301, and 20160302 female bao capsule, linjiang city grand pharmaceutical co., LTD., production batch number of 160202 pu blue tablet, kang county alone blindly biological pharmaceutical co., LTD., production batch number for 1601273001 pieces of ginseng and astragalus fructus schisandrae. The unqualified project has the content determination, microbial limit, the weight difference. 
 
5 batch unqualified drugs list 
药品品名
标示生产企业
生产批号
药品规格
检品来源
检验依据
检验
结果
不合格项目
检验机构
风湿液
天津达仁堂京万红药业有限公司
408513
每瓶装250ml
淄博市第一医院
卫生部药品标准第十七册WS3-B-3160-98
不合格
[含量测定]
宁夏回族自治区药品检验所
汕头市龙湖区第二人民医院(汕头市龙湖区珠池医院)
女宝胶囊
吉林济邦药业有限公司
20160301
每粒装0.3g
湖南同安医药有限公司
卫生部药品标准中药成方制剂第五册
不合格
[检查](微生物限度)
吉林省药品检验所
20160302
包头升华医药有限责任公司
蒲地蓝消炎片
临江市宏大药业有限公司
160202
每片重0.4g
山西潞州中药材开发有限公司长治药品分公司
国家食品药品监督管理局标准YBZ07142008
不合格
[含量测定]
海南省药品检验所
参芪五味子片
康县独一味生物制药有限公司
1601273001
每片重0.26克
宜宾市第二人民医院
国家食品药品监督管理局标准YBZ00312010
不合格
检查(重量差异)
浙江省食品药品检验研究院

For the unqualified drugs, the relevant provinces, autonomous regions and municipalities directly under the food and drug administration has taken seized seized control measures, such as requiring companies to suspend sales use, recalls, and rectification. 
 
CFDA request production enterprises home provinces (autonomous regions and municipalities) food and drug administration of the enterprise on the basis of the pharmaceutical administration law of the People's Republic of China article seventy-four, seventy-four, seventy-five regulations, such as the production and sales of unqualified drugs illegal behavior to carry on the investigation, three months for production and sales of unqualified drugs public enterprises or units deal, and administration of relevant situation report in time. 
 
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