药品说明书是病人治疗用药的依据,是药品生产、经营部门向医药卫生人员和人民群众宣传介绍药品特性,指导合理用药和普及医药卫生知识的主要媒介。按照《药品管理法》及《药品生产质量管理规范》,药品说明书应具有18项内容:品名,主要成份或化学结构式、分子式、分子量,性状,药理 Drug instructions is the basis for the patient’s medication, is the main medium for the pharmaceutical production and operation departments to promote the characteristics of medicines to the medical and health personnel and the public, and to guide the rational use of medicines and popularize the knowledge of medical and health care. According to the “Drug Administration Law” and “Good Manufacturing Practices for Pharmaceutical Production”, the drug specification should have 18 items: name, main component or chemical structure, molecular formula, molecular weight, traits, pharmacology