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
65862-624-05	65862-624	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20150916	N/A	ANDA	ANDA202726	Aurobindo Pharma Limited	GEMFIBROZIL	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-624-05)
65862-624-60	65862-624	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20150916	N/A	ANDA	ANDA202726	Aurobindo Pharma Limited	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-624-60)
0615-8354-39	0615-8354	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20201110	N/A	ANDA	ANDA202726	NCS HealthCare of KY, LLC dba Vangard Labs	GEMFIBROZIL	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8354-39)
71335-2025-1	71335-2025	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20220429	N/A	ANDA	ANDA202726	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2025-1)
71335-2025-2	71335-2025	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20220103	N/A	ANDA	ANDA202726	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2025-2)
71335-2025-3	71335-2025	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240715	N/A	ANDA	ANDA202726	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2025-3)
71335-2025-4	71335-2025	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20220517	N/A	ANDA	ANDA202726	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2025-4)
71335-2025-5	71335-2025	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA202726	Bryant Ranch Prepack	GEMFIBROZIL	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-2025-5)
72603-206-01	72603-206	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20150916	N/A	ANDA	ANDA202726	NorthStar Rx LLC	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72603-206-01)
72603-206-02	72603-206	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20150916	N/A	ANDA	ANDA202726	NorthStar Rx LLC	GEMFIBROZIL	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72603-206-02)
50090-7234-0	50090-7234	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240826	N/A	ANDA	ANDA202726	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7234-0)
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)
53002-2068-6	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)
50090-7233-2	50090-7233	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240826	N/A	ANDA	ANDA202726	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7233-2)
50090-7233-3	50090-7233	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240826	N/A	ANDA	ANDA202726	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7233-3)
50090-7233-4	50090-7233	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240826	N/A	ANDA	ANDA202726	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (50090-7233-4)
50090-7233-0	50090-7233	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20240826	N/A	ANDA	ANDA202726	A-S Medication Solutions	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-7233-0)
16571-784-06	16571-784	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20150916	N/A	ANDA	ANDA202726	Rising Pharma Holdings, Inc.	GEMFIBROZIL	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-784-06)
16571-784-50	16571-784	HUMAN PRESCRIPTION DRUG	Gemfibrozil	Gemfibrozil	TABLET, FILM COATED	ORAL	20150916	N/A	ANDA	ANDA202726	Rising Pharma Holdings, Inc.	GEMFIBROZIL	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-784-50)
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)