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新修订的《中华人民共和国药品管理法》第六章第五十四条规定:药品包装必须按照规定印有或者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有效期。第五章第四十九条规定:禁止生产、销售劣药。同时规定未标明有效期或者更改有效期的;按劣药论处;
The newly revised Article 54 of Chapter VI of the Drug Administration Law of the People’s Republic of China stipulates that the packaging of medicines must be printed or labeled according to relevant regulations and attached with instructions. Labels or instructions must indicate the validity of the drug. Article 49 of the fifth chapter provides: Prohibition of production, sale of inferior drugs. At the same time does not indicate the validity period or change the validity period;