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
71610-532-60	71610-532	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210309	N/A	ANDA	ANDA090796	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-532-60)
71610-532-80	71610-532	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210309	N/A	ANDA	ANDA090796	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-532-80)
71610-532-92	71610-532	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210309	N/A	ANDA	ANDA090796	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71610-532-92)
80425-0243-4	80425-0243	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230110	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)
68071-3362-2	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-3362-2)
68071-3362-3	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3362-3)
68071-3362-4	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (68071-3362-4)
68071-3362-5	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-3362-5)
68071-3362-6	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-3362-6)
68071-3362-9	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3362-9)
73086-210-01	73086-210	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20240320	N/A	ANDA	ANDA090796	SKYA HEALTH, LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (73086-210-01)
71335-1396-7	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)
71335-1396-8	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-8)
71335-1396-9	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1396-9)
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)