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
50580-230-08	50580-230	HUMAN OTC DRUG	Motrin IB	Ibuprofen	TABLET, FILM COATED	ORAL	20170630	N/A	ANDA	ANDA077349	Kenvue Brands LLC	IBUPROFEN	200 mg/1	2 TABLET, FILM COATED in 1 POUCH (50580-230-08)
50580-230-09	50580-230	HUMAN OTC DRUG	Motrin IB	Ibuprofen	TABLET, FILM COATED	ORAL	20170424	N/A	ANDA	ANDA077349	Kenvue Brands LLC	IBUPROFEN	200 mg/1	50 POUCH in 1 CARTON (50580-230-09) / 2 TABLET, FILM COATED in 1 POUCH
50594-005-78	50594-005	HUMAN OTC DRUG	sound body ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20150421	N/A	ANDA	ANDA077349	Big Lots Stores, Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (50594-005-78) / 100 TABLET, FILM COATED in 1 BOTTLE
30142-517-78	30142-517	HUMAN OTC DRUG	ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20060427	N/A	ANDA	ANDA077349	Kroger Company	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (30142-517-78) / 100 TABLET, FILM COATED in 1 BOTTLE
70000-0003-1	70000-0003	HUMAN OTC DRUG	leader ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20191218	N/A	ANDA	ANDA077349	Cardinal Health 110, LLC. dba Leader	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (70000-0003-1) / 50 TABLET, FILM COATED in 1 BOTTLE
70000-0003-2	70000-0003	HUMAN OTC DRUG	leader ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210929	N/A	ANDA	ANDA077349	Cardinal Health 110, LLC. dba Leader	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (70000-0003-2) / 100 TABLET, FILM COATED in 1 BOTTLE