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
71335-0690-1	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0690-1)
71335-0690-5	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180726	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0690-5)
71335-0690-6	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0690-6)
71335-0690-7	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0690-7)
71335-0690-8	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180821	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-0690-8)
71335-0690-9	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180220	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0690-9)
71335-0690-2	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180219	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0690-2)
71335-0690-3	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180227	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-0690-3)
71335-0690-4	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180226	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0690-4)
70518-1051-0	70518-1051	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180301	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1051-0)
70518-1051-2	70518-1051	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20201211	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-2)
70518-1051-4	70518-1051	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-4)
61919-463-21	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (61919-463-21)
61919-463-60	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (61919-463-60)
61919-463-71	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (61919-463-71)
61919-463-72	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (61919-463-72)
61919-463-90	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (61919-463-90)
61919-463-40	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (61919-463-40)
61919-463-45	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (61919-463-45)
61919-463-15	61919-463	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUOROFEN	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA091625	Direct_Rx	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (61919-463-15)