{"topic_id":"cn_vet_drug_regulation_2020","category":"cn-vet-regulation","context":"---\ntopic_id: cn_vet_drug_regulation_2020\ntitle: China — 兽药管理条例（2020年修订版） (Veterinary Drug Regulation, State Council Order No.404, as revised to 2020): licensing, distribution, human-drug ban\ncategory: cn-vet-regulation\nlang: en\nsource_file: pdf-raw/cn-vet-regulation/vet_drug_regulation_2020.txt\nsource_url: https://www.nahs.org.cn/gk/zcjd/202104/t20210407_375367.htm\ndate_parsed: 2026-07-24\ntokens_estimated: 0\nrecovered: false\n---\n\n# China — 兽药管理条例（2020年修订版） (Veterinary Drug Regulation, State Council Order No.404, as revised to 2020): licensing, distribution, human-drug ban\n\nThe <Veterinary Drug Regulation> (兽药管理条例) was initially promulgated as State Council Order No.404 and revised in 2014 (Order No.629), 2016 (Order No.666) and 2020. It is the umbrella law for veterinary-drug production, operation, use and supervision. A veterinary-drug production license is valid 5 years and must be re-applied 6 months before expiry. Veterinary-drug trading enterprises must keep purchase/sales records and are barred from dealing in human drugs or counterfeit/inferior veterinary drugs. (Source is a verbatim republication by the MoA-affiliated China Animal Health and Epidemiology Center / nahs.org.cn.)\n\n## Verified claims (C1 — exact substrings of first-hand Chinese official source)\n\n1. 中文原文：兽药管理条例（2020年修订版）\n2. 中文原文：国务院令第404号发布；根据2014年7月29日《国务院关于修改部分行政法规的决定》第一次修订；根据2016年2月6日国务院令第666号《国务院关于修改部分行政法规的决定》第二次修订；依据2020年3月27日《国务院关于\n3. 中文原文：兽药生产许可证有效期为5年。有效期届满，需要继续生产兽药的，应当在许可证有效期届满前6个月到发证机关申请换发兽药生产许可证。\n4. 中文原文：人用药品和假、劣兽药。\n5. 中文原文：兽药经营企业购销兽药，应当建立购销记录。\n","sources":[],"tokens_estimated":214,"generated_at":null,"tip":"Use /api/v1/topics to discover more topics. /api/v1/nutrient for precise single-point queries. /api/v1/cross_compare for 2-3 standard comparisons."}