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
42806-260-60	42806-260	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20170323	N/A	ANDA	ANDA078012	Epic Pharma, LLC	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (42806-260-60)
42806-260-18	42806-260	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20170323	N/A	ANDA	ANDA078012	Epic Pharma, LLC	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (42806-260-18)
42806-260-05	42806-260	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20170323	N/A	ANDA	ANDA078012	Epic Pharma, LLC	GEMFIBROZIL	600 mg/1	500 TABLET in 1 BOTTLE (42806-260-05)
24658-260-05	24658-260	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20110401	N/A	ANDA	ANDA078012	PuraCap Laboratories LLC dba Blu Pharmaceuticals	GEMFIBROZIL	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-05)
24658-260-90	24658-260	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20110401	N/A	ANDA	ANDA078012	PuraCap Laboratories LLC dba Blu Pharmaceuticals	GEMFIBROZIL	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-90)
24658-260-18	24658-260	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20110401	N/A	ANDA	ANDA078012	PuraCap Laboratories LLC dba Blu Pharmaceuticals	GEMFIBROZIL	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-18)
24658-260-30	24658-260	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20110401	N/A	ANDA	ANDA078012	PuraCap Laboratories LLC dba Blu Pharmaceuticals	GEMFIBROZIL	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-30)
24658-260-60	24658-260	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20110401	N/A	ANDA	ANDA078012	PuraCap Laboratories LLC dba Blu Pharmaceuticals	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-60)
71610-824-30	71610-824	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240429	N/A	ANDA	ANDA078012	Aphena Pharma Solutions - Tennessee, LLC	GEMFIBROZIL	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-824-30)
43063-921-60	43063-921	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20181226	N/A	ANDA	ANDA078012	PD-Rx Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (43063-921-60)
71610-824-53	71610-824	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240429	N/A	ANDA	ANDA078012	Aphena Pharma Solutions - Tennessee, LLC	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-824-53)
71610-824-60	71610-824	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240429	N/A	ANDA	ANDA078012	Aphena Pharma Solutions - Tennessee, LLC	GEMFIBROZIL	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-824-60)
71610-824-80	71610-824	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240429	N/A	ANDA	ANDA078012	Aphena Pharma Solutions - Tennessee, LLC	GEMFIBROZIL	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-824-80)
71335-0051-1	71335-0051	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20171003	N/A	ANDA	ANDA078012	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (71335-0051-1)
71335-0051-5	71335-0051	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20171003	N/A	ANDA	ANDA078012	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (71335-0051-5)
71335-0051-2	71335-0051	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20171003	N/A	ANDA	ANDA078012	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (71335-0051-2)
71335-0051-3	71335-0051	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20171003	N/A	ANDA	ANDA078012	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	100 TABLET in 1 BOTTLE (71335-0051-3)
71335-0051-4	71335-0051	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	GEMFIBROZIL	TABLET	ORAL	20171003	N/A	ANDA	ANDA078012	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (71335-0051-4)