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
53002-2068-6	53002-2068	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20181001	N/A	ANDA	ANDA202726	RPK Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-2068-6)
53002-2068-0	53002-2068	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20181001	N/A	ANDA	ANDA202726	RPK Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (53002-2068-0)
53002-3068-0	53002-3068	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA202726	RPK Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (53002-3068-0)
53002-3068-6	53002-3068	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA202726	RPK Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-3068-6)