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药品标签是药品名称、主要成份、规格、作用与用途、用法与用量、贮藏、批准文号、注册商标、生产批号以及生产厂名的简要明确说明,是指导合理用药的指南,是药品出厂、销售和使用的凭证。因此,药品标签具有专利和法律的特殊意义。对药品标签必须加强管理,做到科学化、规范化。药品标签的管理是全面质量管理的一个重要组成部份。对药品标签的管理,《药品生产质量管理规范》做了明确规定,其第八章第34条规定:“包装材料、标签和说明书应由专人领取、计数发放,领发
Drug label is the name of the drug, the main ingredients, specifications, role and purpose, usage and dosage, storage, approval number, registered trademark, production lot number and manufacturer’s name clearly concise instructions is to guide the rational use of drugs is the drug factory, Sales and use of credentials. Therefore, the drug label has the special meaning of patents and laws. The labeling of medicines must be strengthened to achieve scientific and standardization. Drug label management is an important part of total quality management. The management of drug labels, “Drug Production Quality Management Code,” made it clear that the eighth chapter of Article 34 provides that: "Packaging materials, labels and instructions should be received by the person, the count issued, the hair