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
49483-612-01	49483-612	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20161116	N/A	ANDA	ANDA091237	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-612-01)
49483-612-05	49483-612	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20161116	N/A	ANDA	ANDA091237	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-612-05)
49483-612-34	49483-612	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20240830	N/A	ANDA	ANDA091237	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-612-34)
49483-611-00	49483-611	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20161116	N/A	ANDA	ANDA091237	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	6500 TABLET, FILM COATED in 1 BAG (49483-611-00)
49483-611-05	49483-611	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20161116	N/A	ANDA	ANDA091237	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-611-05)
49483-612-00	49483-612	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20161116	N/A	ANDA	ANDA091237	TIME CAP LABORATORIES,INC	IBUPROFEN	200 mg/1	6500 TABLET, FILM COATED in 1 BAG (49483-612-00)