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
63187-022-90	63187-022	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20140501	N/A	ANDA	ANDA078558	Proficient Rx LP	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (63187-022-90)
50090-6616-0	50090-6616	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230824	N/A	ANDA	ANDA078558	A-S Medication Solutions	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (50090-6616-0)
60687-457-01	60687-457	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20190603	N/A	ANDA	ANDA078558	American Health Packaging	IBUPROFEN	600 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-457-01) / 1 TABLET in 1 BLISTER PACK (60687-457-11)
60687-468-01	60687-468	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20200325	N/A	ANDA	ANDA078558	American Health Packaging	IBUPROFEN	800 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-468-01) / 1 TABLET in 1 BLISTER PACK (60687-468-11)
53746-464-01	53746-464	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (53746-464-01)