根据《药品注册管理办法》，申请人拟在进口药品批准证明文件有效期期满后继续进口该药品的注册申请属于\n \n \n

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\n \n A、仿制药申请

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\n \n B、再注册申请

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\n \n C、进口药品申请

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\n \n D、补充申请