《中华人民共和国药典》九五版二部凡例二十三条规定:药品标签应符合《中华人民共和国药品管理法》对标签的规定,其内容应包括法定通用名称、规格、装量、生产企业、批准文号、产品主要成分、适应症、用法用量、注意事项、有效期(或使用期)及贮藏条件等。查阅有关规定,均未要求在药品标签上注明厂负责期。药品的厂负责期是药品生产 The twenty-seventh edition of the “Pharmacopoeia of the People’s Republic of China”, Part Nine of the twenty-fifth edition, stipulates that Article 23 of the Pharmacopoeia shall comply with the “Laboratory Regulations of the People’s Republic of China” on the label, and the content shall include the legally-accepted common name, specifications, quantity, and manufacturer , approval number, major components of the product, indications, dosage, precautions, expiration date (or use period), and storage conditions. Check the relevant provisions, have not required to indicate on the drug label factory responsible period. The drug factory is responsible for drug production