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
80425-0501-8	80425-0501	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250213	N/A	ANDA	ANDA076003	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	240 TABLET, COATED in 1 BOTTLE (80425-0501-8)
60219-2348-1	60219-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, COATED in 1 BOTTLE (60219-2348-1)
60219-2348-4	60219-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	10 TABLET, COATED in 1 BOTTLE (60219-2348-4)
60219-2348-5	60219-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, COATED in 1 BOTTLE (60219-2348-5)
60219-2348-7	60219-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, COATED in 1 BOTTLE (60219-2348-7)