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
71335-1396-1	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)
71335-1396-2	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)
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)
53002-3981-5	53002-3981	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA090796	RPK Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (53002-3981-5)
45865-945-30	45865-945	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20181212	N/A	ANDA	ANDA090796	medsource pharmaceuticals	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (45865-945-30)
45865-945-60	45865-945	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20181212	N/A	ANDA	ANDA090796	medsource pharmaceuticals	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (45865-945-60)
70518-0005-6	70518-0005	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20230317	N/A	ANDA	ANDA090796	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0005-6)
68071-4459-6	68071-4459	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
68071-5134-6	68071-5134	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191213	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-5134-6)
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)
68071-5140-3	68071-5140	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191231	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (68071-5140-3)
68071-5140-6	68071-5140	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200106	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-5140-6)
63187-451-40	63187-451	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20190101	N/A	ANDA	ANDA090796	Proficient Rx LP	IBUPROFEN	600 mg/1	40 TABLET in 1 BOTTLE (63187-451-40)
63187-451-60	63187-451	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20190101	N/A	ANDA	ANDA090796	Proficient Rx LP	IBUPROFEN	600 mg/1	60 TABLET in 1 BOTTLE (63187-451-60)
63187-451-90	63187-451	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20190101	N/A	ANDA	ANDA090796	Proficient Rx LP	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (63187-451-90)