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
59556-805-06	59556-805	HUMAN OTC DRUG	IBUPROFEN IMMEDIATE RELEASE	IBUPROFEN	TABLET, COATED	ORAL	20160826	N/A	ANDA	ANDA207052	Strides Pharma Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (59556-805-06) / 100 TABLET, COATED in 1 BOTTLE
59556-805-08	59556-805	HUMAN OTC DRUG	IBUPROFEN IMMEDIATE RELEASE	IBUPROFEN	TABLET, COATED	ORAL	20160826	N/A	ANDA	ANDA207052	Strides Pharma Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (59556-805-08) / 1000 TABLET, COATED in 1 BOTTLE
59556-805-41	59556-805	HUMAN OTC DRUG	IBUPROFEN IMMEDIATE RELEASE	IBUPROFEN	TABLET, COATED	ORAL	20160826	N/A	ANDA	ANDA207052	Strides Pharma Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (59556-805-41) / 24 TABLET, COATED in 1 BOTTLE
59556-806-06	59556-806	HUMAN OTC DRUG	IBUPROFEN IMMEDIATE RELEASE	IBUPROFEN	TABLET, COATED	ORAL	20160826	N/A	ANDA	ANDA207052	Strides Pharma Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (59556-806-06) / 100 TABLET, COATED in 1 BOTTLE
59556-806-08	59556-806	HUMAN OTC DRUG	IBUPROFEN IMMEDIATE RELEASE	IBUPROFEN	TABLET, COATED	ORAL	20160826	N/A	ANDA	ANDA207052	Strides Pharma Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (59556-806-08) / 1000 TABLET, COATED in 1 BOTTLE
59556-806-41	59556-806	HUMAN OTC DRUG	IBUPROFEN IMMEDIATE RELEASE	IBUPROFEN	TABLET, COATED	ORAL	20160826	N/A	ANDA	ANDA207052	Strides Pharma Inc.	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (59556-806-41) / 24 TABLET, COATED in 1 BOTTLE
72927-805-01	72927-805	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20190910	N/A	ANDA	ANDA207052	Strides Consumer LLC	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (72927-805-01) / 120 TABLET, COATED in 1 BOTTLE
72927-805-02	72927-805	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20190910	N/A	ANDA	ANDA207052	Strides Consumer LLC	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (72927-805-02) / 24 TABLET, COATED in 1 BOTTLE