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
53746-617-01	53746-617	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20091217	N/A	ANDA	ANDA090485	Amneal Pharmaceuticals of New York LLC	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	100 TABLET in 1 BOTTLE (53746-617-01)
53746-617-05	53746-617	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20091217	N/A	ANDA	ANDA090485	Amneal Pharmaceuticals of New York LLC	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	500 TABLET in 1 BOTTLE (53746-617-05)
53746-617-10	53746-617	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20091217	N/A	ANDA	ANDA090485	Amneal Pharmaceuticals of New York LLC	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	1000 TABLET in 1 BOTTLE (53746-617-10)
53746-617-30	53746-617	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20091217	N/A	ANDA	ANDA090485	Amneal Pharmaceuticals of New York LLC	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	30 TABLET in 1 BOTTLE (53746-617-30)