美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
80425-0057-1	80425-0057	HUMAN PRESCRIPTION DRUG	Tramadol HCL	Tramadol HCL	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, COATED in 1 BOTTLE (80425-0057-1)
80425-0057-2	80425-0057	HUMAN PRESCRIPTION DRUG	Tramadol HCL	Tramadol HCL	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, COATED in 1 BOTTLE (80425-0057-2)
80425-0057-3	80425-0057	HUMAN PRESCRIPTION DRUG	Tramadol HCL	Tramadol HCL	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, COATED in 1 BOTTLE (80425-0057-3)
80425-0057-4	80425-0057	HUMAN PRESCRIPTION DRUG	Tramadol HCL	Tramadol HCL	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	15 TABLET, COATED in 1 BOTTLE (80425-0057-4)
80425-0057-5	80425-0057	HUMAN PRESCRIPTION DRUG	Tramadol HCL	Tramadol HCL	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, COATED in 1 BOTTLE (80425-0057-5)
0904-7496-61	0904-7496	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20241122	N/A	ANDA	ANDA076003	Major Pharmaceuticals	TRAMADOL HYDROCHLORIDE	50 mg/1	100 BLISTER PACK in 1 CARTON (0904-7496-61) / 1 TABLET, COATED in 1 BLISTER PACK