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
51655-474-52	51655-474	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210114	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-52)
72189-324-60	72189-324	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA090796	Direct Rx	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-324-60)
51655-275-20	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210709	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
51655-275-21	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20201029	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)
51655-275-25	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210217	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-25)
51655-275-26	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20200616	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26)
51655-275-54	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20200921	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-54)
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)
25000-121-03	25000-121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	400 mg/1	30 TABLET in 1 BOTTLE (25000-121-03)
25000-121-12	25000-121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	400 mg/1	500 TABLET in 1 BOTTLE (25000-121-12)
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)
68071-5126-3	68071-5126	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191211	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-5126-3)