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
41226-600-01	41226-600	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20210612	N/A	ANDA	ANDA091239	Kroger Company	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (41226-600-01) / 100 TABLET, COATED in 1 BOTTLE
41226-600-42	41226-600	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20210612	N/A	ANDA	ANDA091239	Kroger Company	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (41226-600-42) / 24 TABLET, COATED in 1 BOTTLE
41226-600-50	41226-600	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20210612	N/A	ANDA	ANDA091239	Kroger Company	IBUPROFEN	200 mg/1	500 TABLET, COATED in 1 BOTTLE (41226-600-50)
49483-600-01	49483-600	HUMAN OTC DRUG	IBUPROFEN	IBUPFROFEN	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-600-01)
49483-600-05	49483-600	HUMAN OTC DRUG	IBUPROFEN	IBUPFROFEN	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-600-05)
49483-600-50	49483-600	HUMAN OTC DRUG	IBUPROFEN	IBUPFROFEN	TABLET, FILM COATED	ORAL	20171114	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (49483-600-50)
49483-601-00	49483-601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	6500 TABLET, FILM COATED in 1 BAG (49483-601-00)
49483-601-01	49483-601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-601-01)
49483-601-05	49483-601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-601-05)
11822-7891-2	11822-7891	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	50 TABLET, COATED in 1 BOTTLE (11822-7891-2)
11822-7891-5	11822-7891	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	100 TABLET, COATED in 1 BOTTLE (11822-7891-5)
11822-7891-9	11822-7891	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	500 TABLET, COATED in 1 BOTTLE (11822-7891-9)
11822-7892-0	11822-7892	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	24 TABLET, COATED in 1 BOTTLE (11822-7892-0)
11822-7892-2	11822-7892	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	50 TABLET, COATED in 1 BOTTLE (11822-7892-2)
11822-7892-5	11822-7892	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	100 TABLET, COATED in 1 BOTTLE (11822-7892-5)
11822-7892-7	11822-7892	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	200 TABLET, COATED in 1 BOTTLE (11822-7892-7)
11822-7892-9	11822-7892	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091239	RITE AID CORPORATION	IBUPROFEN	200 mg/1	500 TABLET, COATED in 1 BOTTLE (11822-7892-9)