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
71335-1902-1	71335-1902	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20210713	N/A	ANDA	ANDA203266	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (71335-1902-1)
71335-1902-2	71335-1902	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20210803	N/A	ANDA	ANDA203266	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	30 TABLET in 1 BOTTLE (71335-1902-2)
71335-1902-3	71335-1902	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20220310	N/A	ANDA	ANDA203266	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	100 TABLET in 1 BOTTLE (71335-1902-3)
71335-1902-4	71335-1902	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20220310	N/A	ANDA	ANDA203266	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	90 TABLET in 1 BOTTLE (71335-1902-4)
71335-1902-5	71335-1902	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20210913	N/A	ANDA	ANDA203266	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (71335-1902-5)
75834-131-05	75834-131	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20170215	N/A	ANDA	ANDA203266	Nivagen Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	500 TABLET in 1 BOTTLE (75834-131-05)
75834-131-18	75834-131	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20170215	N/A	ANDA	ANDA203266	Nivagen Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (75834-131-18)
75834-131-60	75834-131	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20170215	N/A	ANDA	ANDA203266	Nivagen Pharmaceuticals, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (75834-131-60)
71209-008-03	71209-008	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20181017	N/A	ANDA	ANDA203266	Cadila Pharmaceuticals Limited	GEMFIBROZIL	600 mg/1	60 TABLET in 1 BOTTLE (71209-008-03)
71209-008-08	71209-008	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20181017	N/A	ANDA	ANDA203266	Cadila Pharmaceuticals Limited	GEMFIBROZIL	600 mg/1	180 TABLET in 1 BOTTLE (71209-008-08)
71209-008-10	71209-008	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET	ORAL	20181017	N/A	ANDA	ANDA203266	Cadila Pharmaceuticals Limited	GEMFIBROZIL	600 mg/1	500 TABLET in 1 BOTTLE (71209-008-10)