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
53746-137-01	53746-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20090105	N/A	ANDA	ANDA071935	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (53746-137-01)
53746-137-05	53746-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20090105	N/A	ANDA	ANDA071935	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	500 TABLET in 1 BOTTLE (53746-137-05)
53746-137-30	53746-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20090105	N/A	ANDA	ANDA071935	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (53746-137-30)
53746-137-50	53746-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20090105	N/A	ANDA	ANDA071935	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	50 TABLET in 1 BOTTLE (53746-137-50)
53746-137-60	53746-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20090105	N/A	ANDA	ANDA071935	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (53746-137-60)
53746-137-90	53746-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20090105	N/A	ANDA	ANDA071935	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (53746-137-90)