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
63187-063-78	63187-063	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20140501	N/A	ANDA	ANDA076003	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	180 TABLET, COATED in 1 BOTTLE (63187-063-78)
63187-063-90	63187-063	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20140501	N/A	ANDA	ANDA076003	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, COATED in 1 BOTTLE (63187-063-90)
63187-063-40	63187-063	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20140501	N/A	ANDA	ANDA076003	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	40 TABLET, COATED in 1 BOTTLE (63187-063-40)
63187-063-15	63187-063	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20170801	N/A	ANDA	ANDA076003	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	15 TABLET, COATED in 1 BOTTLE (63187-063-15)
63187-063-20	63187-063	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20161101	N/A	ANDA	ANDA076003	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET, COATED in 1 BOTTLE (63187-063-20)