# China NMPA Drug Inspection - Chengdu Hexiangtian Pharmaceutical Co., Ltd. - Children's oral liquid for clearing heat and relieving cough

Source: https://www.globalkeysolutions.net/records/china_drug_inspection/chengdu-hexiangtian-pharmaceutical-co-ltd/9888a42c-7c7f-47fb-8b13-ae18ed8f07a6/
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> China NMPA drug inspection for Chengdu Hexiangtian Pharmaceutical Co., Ltd. published January 05, 2018. Drug: Children's oral liquid for clearing heat and relieving cough. The National Medical Products Administration (NMPA) of China issued Announcement No. 5 of 2018 on January 5, 2018, repor

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## Details

- Record Type: CHINA_DRUG_INSPECTION
- Title: Announcement No. 5 of 2018 from the State Administration for Market Regulation regarding 20 batches of substandard drugs.
- Company Name: Chengdu Hexiangtian Pharmaceutical Co., Ltd.
- Publication Date: 2018-01-05
- Drug Name: Children's oral liquid for clearing heat and relieving cough
- Inspection Finding: [Check] (Quantity)
- Action Taken: Relevant provincial-level food and drug administration departments have taken control measures such as sealing and seizing goods, requiring enterprises to suspend sales and use, recall products, and rectify the situation. The State Food and Drug Administration has instructed the provincial-level food and drug administration departments where the relevant units are located to investigate the illegal acts of producing and selling substandard drugs by the aforementioned enterprises in accordance with Articles 73, 74, and 75 of the "Drug Administration Law of the People's Republic of China," and to publicly disclose the results of the handling of the relevant enterprises or units producing and selling substandard drugs within three months, and to promptly report the relevant information to the State Food and Drug Administration.
- Summary: The National Medical Products Administration (NMPA) of China issued Announcement No. 5 of 2018 on January 5, 2018, reporting 20 batches of substandard drugs from 12 manufacturers. The findings stemmed from testing conducted by five drug testing institutions, including the Guizhou Provincial Institute for Food and Drug Control. Key companies identified include Jiangxi Yongsheng Biochemical Pharmaceutical Co., Ltd., Wuhan Kangle Pharmaceutical Co., Ltd., Chengdu Zhengkang Pharmaceutical Co., Ltd., Diaoyutai Pharmaceutical Group Jilin Tianqi Pharmaceutical Co., Ltd., and Jilin Wantong Pharmaceutical Group Meihe Pharmaceutical Co., Ltd., among others. The substandard products encompassed various pharmaceutical forms, such as oral solutions, capsules, and tablets. The primary issues discovered included critical quality deviations such as incorrect fill volume, insufficient or incorrect content determination (e.g., active ingredients like camphor or toad venom), excessive moisture content, non-compliance with microbial limits, and unacceptable weight variation in tablets. In response, provincial food and drug administrations implemented immediate control measures, including sealing and seizing affected products, mandating sales suspension, product recalls, and requiring manufacturers to rectify the identified problems. Furthermore, the NMPA directed provincial authorities to investigate these illegal activities in accordance with Articles 73, 74, and 75 of the *Drug Administration Law of the People's Republic of China*. The results of these investigations and the subsequent handling of the enterprises must be publicly disclosed within three months, with reports submitted to the NMPA.

Company: https://www.globalkeysolutions.net/companies/chengdu-hexiangtian-pharmaceutical-co-ltd/efaf36e0-7185-4df1-9f49-c6f2f680b3f5/