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
71335-1503-6	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6)
71335-1503-7	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7)
71335-1503-8	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-1503-8)
71335-1503-9	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1503-9)
67296-1584-1	67296-1584	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	600 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (67296-1584-1)
67296-1584-3	67296-1584	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1584-3)
80425-0426-1	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (80425-0426-1)
80425-0426-2	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	60 TABLET in 1 BOTTLE (80425-0426-2)
80425-0426-3	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (80425-0426-3)
80425-0426-4	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (80425-0426-4)
71335-1517-1	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)
71335-1517-2	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2)
71335-1517-3	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3)
71335-1517-4	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4)
71335-1517-5	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5)
71335-1517-6	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6)
71335-1517-7	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7)
71335-1517-8	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8)
71335-1517-9	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9)
67296-1685-2	67296-1685	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (67296-1685-2)