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
68788-6447-6	68788-6447	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20160802	N/A	ANDA	ANDA077836	Preferred Pharmaceuticals Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (68788-6447-6)
68788-6447-3	68788-6447	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20160802	N/A	ANDA	ANDA077836	Preferred Pharmaceuticals Inc.	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (68788-6447-3)
70518-1563-1	70518-1563	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20181023	N/A	ANDA	ANDA077836	REMEDYREPACK INC.	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BLISTER PACK (70518-1563-1)
70518-1563-4	70518-1563	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20250428	N/A	ANDA	ANDA077836	REMEDYREPACK INC.	GEMFIBROZIL	600 mg/1	100 POUCH in 1 BOX (70518-1563-4) / 1 TABLET in 1 POUCH (70518-1563-5)
70518-1563-6	70518-1563	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20250701	N/A	ANDA	ANDA077836	REMEDYREPACK INC.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (70518-1563-6)
69097-821-03	69097-821	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20161013	N/A	ANDA	ANDA077836	Cipla USA Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (69097-821-03)
69097-821-07	69097-821	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20161013	N/A	ANDA	ANDA077836	Cipla USA Inc.	GEMFIBROZIL	600 mg/1	100 TABLET in 1 BOTTLE (69097-821-07)
69097-821-12	69097-821	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20161013	N/A	ANDA	ANDA077836	Cipla USA Inc.	GEMFIBROZIL	600 mg/1	500 TABLET in 1 BOTTLE (69097-821-12)
60687-224-01	60687-224	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20160707	N/A	ANDA	ANDA077836	American Health Packaging	GEMFIBROZIL	600 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-224-01) / 1 TABLET in 1 BLISTER PACK (60687-224-11)
76282-225-05	76282-225	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20061020	N/A	ANDA	ANDA077836	Exelan Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76282-225-05)
76282-225-18	76282-225	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20061020	N/A	ANDA	ANDA077836	Exelan Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (76282-225-18)
76282-225-60	76282-225	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20061020	N/A	ANDA	ANDA077836	Exelan Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76282-225-60)