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药品管理法第三十六条规定:“药品包装必须适合药品质量的要求,方便储存、运输和医疗使用。规定有效期的药品,必须在包装上注明有效期。”第三十七条规定:“药品包装必须按照规定贴有标签并附有说明书,标签或者说明书上,必须注明药品的品名、规格、生产企业批准文号、产品批号、主要成分、适应证、用法、用量、禁忌、不良反应和注意事项。麻醉药品、精神药品、毒性药品的标签必须印有规定的标志。”
Article 36 of the Drug Administration Law stipulates: “The packaging of pharmaceuticals must be suitable for the requirements of the quality of medicines, and it is convenient for storage, transportation, and medical use. For drugs that are required to have an effective period of time, the period of validity must be stated on the packaging.” Article 37 states: “ The medicine packaging must be affixed with the label in accordance with the regulations and attached with the instructions. The label or the instruction must indicate the name of the medicine, the specifications, the approval number of the manufacturer, the batch number of the product, the main ingredients, the indication, usage, dosage, taboo, and adverse reactions. And precautions. Labels for narcotic drugs, psychotropic substances, and toxic drugs must bear the prescribed signs.”