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
72162-2119-6	72162-2119	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20230915	N/A	ANDA	ANDA214603	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (72162-2119-6)
72865-186-05	72865-186	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210120	N/A	ANDA	ANDA214603	XLCare Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	500 TABLET in 1 BOTTLE (72865-186-05)
72865-186-18	72865-186	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210120	N/A	ANDA	ANDA214603	XLCare Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (72865-186-18)
72865-186-60	72865-186	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210120	N/A	ANDA	ANDA214603	XLCare Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (72865-186-60)
31722-128-05	31722-128	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210120	N/A	ANDA	ANDA214603	Camber Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	500 TABLET in 1 BOTTLE (31722-128-05)
31722-128-60	31722-128	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210120	N/A	ANDA	ANDA214603	Camber Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (31722-128-60)
71610-601-53	71610-601	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20211019	N/A	ANDA	ANDA214603	Aphena Pharma Solutions - Tennessee, LLC	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (71610-601-53)
71610-601-60	71610-601	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20211006	N/A	ANDA	ANDA214603	Aphena Pharma Solutions - Tennessee, LLC	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (71610-601-60)
68788-7964-3	68788-7964	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210720	N/A	ANDA	ANDA214603	Preferred Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (68788-7964-3)
68788-7964-6	68788-7964	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210720	N/A	ANDA	ANDA214603	Preferred Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (68788-7964-6)
68788-7964-9	68788-7964	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210720	N/A	ANDA	ANDA214603	Preferred Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (68788-7964-9)
43602-452-10	43602-452	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210113	N/A	ANDA	ANDA214603	Ascent Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	1000 TABLET in 1 BOTTLE (43602-452-10)
43602-452-30	43602-452	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20210113	N/A	ANDA	ANDA214603	Ascent Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (43602-452-30)
71335-1996-1	71335-1996	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20220210	N/A	ANDA	ANDA214603	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (71335-1996-1)
71335-1996-2	71335-1996	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20220210	N/A	ANDA	ANDA214603	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (71335-1996-2)
71335-1996-3	71335-1996	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20220210	N/A	ANDA	ANDA214603	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	100 TABLET in 1 BOTTLE (71335-1996-3)
71335-1996-4	71335-1996	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20220210	N/A	ANDA	ANDA214603	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (71335-1996-4)
71335-1996-5	71335-1996	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20220210	N/A	ANDA	ANDA214603	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (71335-1996-5)
50090-5808-0	50090-5808	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20211015	N/A	ANDA	ANDA214603	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (50090-5808-0)
50090-5808-2	50090-5808	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20211015	N/A	ANDA	ANDA214603	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (50090-5808-2)