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
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)
0363-9601-01	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0363-9601-01)
0363-9601-05	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	50 TABLET in 1 BOTTLE, PLASTIC (0363-9601-05)
0363-9601-10	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0363-9601-10)
0363-9601-15	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	150 TABLET in 1 BOTTLE, PLASTIC (0363-9601-15)
0363-9601-20	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20251001	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	200 TABLET in 1 BOTTLE, PLASTIC (0363-9601-20)
0363-9601-42	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	24 TABLET in 1 BOTTLE, PLASTIC (0363-9601-42)
0363-9601-50	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (0363-9601-50)
0363-9601-97	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	2 BOTTLE in 1 CARTON (0363-9601-97) / 100 TABLET in 1 BOTTLE
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)
49483-114-10	49483-114	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210909	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (49483-114-10)
11673-990-20	11673-990	HUMAN OTC DRUG	IBUPROFEN CA	IBUPROFEN	TABLET, COATED	ORAL	20200101	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	200 TABLET, COATED in 1 BOTTLE (11673-990-20)
11673-990-42	11673-990	HUMAN OTC DRUG	IBUPROFEN CA	IBUPROFEN	TABLET, COATED	ORAL	20200101	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	24 TABLET, COATED in 1 BOTTLE (11673-990-42)
49483-114-17	49483-114	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230819	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	200 TABLET, FILM COATED in 1 BOTTLE (49483-114-17)
49483-114-50	49483-114	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210909	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (49483-114-50)
49483-114-73	49483-114	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20231118	N/A	ANDA	ANDA091239	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-114-73)
25000-114-02	25000-114	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20191220	N/A	ANDA	ANDA091239	MARKSANS PHARMA LIMITED	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (25000-114-02) / 24 TABLET in 1 BOTTLE