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
71610-547-60	71610-547	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210430	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (71610-547-60)
71610-547-80	71610-547	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210430	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	180 TABLET in 1 BOTTLE (71610-547-80)
71610-547-92	71610-547	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210430	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	270 TABLET in 1 BOTTLE (71610-547-92)
71610-550-60	71610-550	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210501	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (71610-550-60)
71610-550-80	71610-550	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210501	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	180 TABLET in 1 BOTTLE (71610-550-80)
71610-550-92	71610-550	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210501	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	270 TABLET in 1 BOTTLE (71610-550-92)
71205-604-15	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	15 TABLET in 1 BOTTLE (71205-604-15)
71205-604-20	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	20 TABLET in 1 BOTTLE (71205-604-20)
71205-604-21	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	21 TABLET in 1 BOTTLE (71205-604-21)
71205-604-30	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210827	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	30 TABLET in 1 BOTTLE (71205-604-30)
71205-604-40	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	40 TABLET in 1 BOTTLE (71205-604-40)
71205-604-60	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210827	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	60 TABLET in 1 BOTTLE (71205-604-60)
71205-604-90	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210827	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	90 TABLET in 1 BOTTLE (71205-604-90)
66267-963-00	66267-963	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20170915	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (66267-963-00)
66267-964-00	66267-964	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20170822	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals Inc.	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (66267-964-00)
61919-960-21	61919-960	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20190820	N/A	ANDA	ANDA075682	Direct_Rx	IBUPROFEN	600 mg/1	21 TABLET in 1 BOTTLE (61919-960-21)
61919-960-72	61919-960	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20190820	N/A	ANDA	ANDA075682	Direct_Rx	IBUPROFEN	600 mg/1	120 TABLET in 1 BOTTLE (61919-960-72)
53002-3010-1	53002-3010	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20171001	N/A	ANDA	ANDA075682	RPK Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	10 TABLET in 1 BOTTLE (53002-3010-1)
53002-3010-2	53002-3010	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20171001	N/A	ANDA	ANDA075682	RPK Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	15 TABLET in 1 BOTTLE (53002-3010-2)
53002-3010-3	53002-3010	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20171001	N/A	ANDA	ANDA075682	RPK Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	20 TABLET in 1 BOTTLE (53002-3010-3)