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
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)
82804-221-90	82804-221	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20250424	N/A	ANDA	ANDA214603	Proficient Rx LP	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (82804-221-90)
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)
50090-5808-3	50090-5808	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20211015	N/A	ANDA	ANDA214603	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (50090-5808-3)
50090-5808-4	50090-5808	HUMAN PRESCRIPTION DRUG	GEMFIBROZIL	Gemfibrozil	TABLET	ORAL	20211015	N/A	ANDA	ANDA214603	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (50090-5808-4)