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
68071-4119-9	68071-4119	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20171016	N/A	ANDA	ANDA076003	NuCare Pharmaceuticals,Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, COATED in 1 BOTTLE (68071-4119-9)
69238-2348-1	69238-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, COATED in 1 BOTTLE (69238-2348-1)
69238-2348-4	69238-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	10 TABLET, COATED in 1 BOTTLE (69238-2348-4)
69238-2348-5	69238-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, COATED in 1 BOTTLE (69238-2348-5)
69238-2348-7	69238-2348	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20101115	N/A	ANDA	ANDA076003	Amneal Pharmaceuticals NY LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, COATED in 1 BOTTLE (69238-2348-7)