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
51655-759-52	51655-759	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA090796	Northwind Pharmaceuticals	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-759-52)
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)
53002-3981-1	53002-3981	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA090796	RPK Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (53002-3981-1)
53002-3981-2	53002-3981	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA090796	RPK Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (53002-3981-2)
53002-3981-3	53002-3981	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA090796	RPK Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-3981-3)
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)
68071-3362-0	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (68071-3362-0)
68071-3362-1	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (68071-3362-1)
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)
25000-122-03	25000-122	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (25000-122-03)
25000-122-12	25000-122	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	600 mg/1	500 TABLET in 1 BOTTLE (25000-122-12)
63187-451-30	63187-451	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20190101	N/A	ANDA	ANDA090796	Proficient Rx LP	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (63187-451-30)
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)
67296-1756-1	67296-1756	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200101	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (67296-1756-1)
67296-1756-3	67296-1756	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200101	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1756-3)
49483-603-01	49483-603	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-603-01)
25000-123-03	25000-123	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (25000-123-03)
25000-123-12	25000-123	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	800 mg/1	500 TABLET in 1 BOTTLE (25000-123-12)