A batch of drug sampling unqualified, involving 12 OTC varieties

A batch of drug sampling is unqualified, involving 12 OTC varieties, including calcium gluconate oral solution, cold cough syrup, kidney strength tablets, compound orange terrier cough tablets, fire tablets, compound winter grass tablets ..On November 26th, the State DrugAdministration issued a circular on non-compliance with drug No85 of 2019The circular said that by the Suzhou Drug Inspection and Testing Research Center and other 11 drug inspection institutions, marked as Compaq Pharmaceutical Co., Ltdand other 40 enterprises produced 57 batches of drugs do not meet the regulationscombing found that 57 batches of non-conforming drugs, 11 batches for preparation, 46 batches for Chinese medicine tabletsIt is worth noting that this includes two OTCs, an oral solution of calcium gluconate, a cold cough syrup, and three prescription drugs, respectively, aweitric pyridoxine tablets, inhalation of acetylcysteine solution, and ethyl hydrochloride tabletsnotice that the above-mentioned non-compliant drugs, the drug supervision and administration department has asked the relevant enterprises and units to take suspension of sales, use, recall and other risk control measures, the reasons for non-compliance to carry out investigation and effective rectificationthe State Drug Administration requires the relevant provincial drug regulatory departments to organize an investigation into the illegal acts of the production and sale of counterfeit and inferior drugs by the above-mentioned enterprises and units in accordance with the Drug Administration Law of the People's Republic of China, and to complete the investigation and treatment of the relevant enterprises or units within 3 months from the date of receipt of the inspection report and make public the resultsin the investigation of the case, if the enterprise has any objection to the authenticity of the product, it may submit it to the provincial drug supervision and administration department where it is locatedThe provincial drug supervision and administration department where the production enterprise is located shall investigate and verify the production and sales situation of the enterprise, and the provincial drug supervision and administration department where the sampled unit is located shall trace the source of the product in question;10 OTCsNovember 25, the Guangdong Provincial Drug Administration announced the 7th issue of 2019 drug spot test information noticeIn June 2019, the province conducted spot checks and inspected a total of 1,607 batches of 716 varieties of 64 pharmaceutical manufacturing enterprises, 499 pharmaceutical enterprises and 154 medical institutions, the circular saidverified that 18 varieties of 18 batches have been tested to not meet the requirements of drug standards, of which 15 varieties from the circulation link, 3 varieties from the use of linksAs for the non-conformity factors, mainly for the characteristics, moisture, identification, weight differences, content determination, loading, microbial limits and so onSaiper Blue - pharmacy manager combing found that in the circulation of 15 unqualified drugs, the samples are basically from retail pharmacies, and there are 9 for pharmacies often sell OTC, respectively, Ai warm palace pills, kidney strength tablets, intestinal Thai compound, deaf left Tzu pills, compound orange terrier cough tablets, flat stomach tablets, fire tablets , the intestinal capsule, compound winter grass tablets; the other 6 are prescription drugs, respectively, acetate fluorine easily cream, large detox capsule, milktablets, saline live blood tablets, sugar urine tablets, yanning tablets;it is worth noting that Ai warm palace pills (Shanxi Huakang), the kidney strength tablets (Hubei won), the fire tablets (Guangxi Saint-Min), Yan Ning tablets (Guizhou Sanrentang) and other 4 drugs by the local regulatory authorities to the production enterprises to leave samples to verify the inspection passed, which also said that the four drug production there is no problem, there may be business enterprises circulation, storage, maintenance problemsFor the above non-conforming drugs, the Bureau instructs the relevant municipal market supervision bureau to take the necessary control measures such as seizure, seizure, suspension of sales and recall of unqualified drugs, and to investigate and punish the production enterprises and the units under sampling in accordance with relevant laws and regulations, and to continue to follow up and test these drugsat the same time, the bureau reminded that consumers in the legal formal medical institutions, pharmacies, etcto purchase drugs and ask for the preservation of relevant certificates;if necessary, you can visit the basic database of the State Drug Administration (CFDA) (http://If you purchase counterfeit or substandard drugs, please call the local market regulator y12331 to report the complaint.