根据药品管理法规定擅自添加什么及辅料的按照劣药处理-法规政策咨询及电话投诉类法律援助-法律咨询免费平台-国际律师联盟

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问题	根据药品管理法规定擅自添加什么及辅料的按照劣药处理
释义	法律分析：擅自添加着色剂、防腐剂、香料、矫味剂及辅料的按照劣药处理。法律依据：《中华人民共和国药品管理法》第四十九条禁止生产、销售劣药。药品成分的含量不符合国家药品标准的，为劣药。有下列情形之一的药品，按劣药论处：（1）未标明有效期或者更改有效期的；（2）不注明或者更改生产批号的；（3）超过有效期的；（4）直接接触药品的包装材料和容器未经批准的；（5）擅自添加着色剂、防腐剂、香料、矫味剂及辅料的；（6）其它不符合药品标准规定的。
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