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
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)
68071-4009-1	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (68071-4009-1)
68071-4009-2	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-4009-2)
68071-4009-3	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4009-3)
68071-4009-4	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (68071-4009-4)
68071-4009-5	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (68071-4009-5)
68071-4009-6	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-4009-6)
68071-4009-7	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-4009-7)
68071-4009-9	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-4009-9)
71335-1396-3	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)
71335-1396-4	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)
71335-1396-5	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)
71335-1396-6	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)
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)