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)
检索条件:" 注册申请号=ANDA214603"
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
43602-452-10 43602-452 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210113 N/A ANDA ANDA214603 Ascent Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 1000 TABLET in 1 BOTTLE (43602-452-10)
43602-452-30 43602-452 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210113 N/A ANDA ANDA214603 Ascent Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 30 TABLET in 1 BOTTLE (43602-452-30)
68788-7964-3 68788-7964 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210720 N/A ANDA ANDA214603 Preferred Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 30 TABLET in 1 BOTTLE (68788-7964-3)
68788-7964-6 68788-7964 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210720 N/A ANDA ANDA214603 Preferred Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 60 TABLET in 1 BOTTLE (68788-7964-6)
68788-7964-9 68788-7964 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210720 N/A ANDA ANDA214603 Preferred Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 90 TABLET in 1 BOTTLE (68788-7964-9)
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)
71610-601-53 71610-601 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20211019 N/A ANDA ANDA214603 Aphena Pharma Solutions - Tennessee, LLC GEMFIBROZIL 600 mg/1 60 TABLET in 1 BOTTLE (71610-601-53)
71610-601-60 71610-601 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20211006 N/A ANDA ANDA214603 Aphena Pharma Solutions - Tennessee, LLC GEMFIBROZIL 600 mg/1 90 TABLET in 1 BOTTLE (71610-601-60)
31722-128-05 31722-128 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210120 N/A ANDA ANDA214603 Camber Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 500 TABLET in 1 BOTTLE (31722-128-05)
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)
72162-2119-6 72162-2119 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20230915 N/A ANDA ANDA214603 Bryant Ranch Prepack GEMFIBROZIL 600 mg/1 60 TABLET in 1 BOTTLE (72162-2119-6)
72865-186-05 72865-186 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210120 N/A ANDA ANDA214603 XLCare Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 500 TABLET in 1 BOTTLE (72865-186-05)
72865-186-18 72865-186 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210120 N/A ANDA ANDA214603 XLCare Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 180 TABLET in 1 BOTTLE (72865-186-18)
72865-186-60 72865-186 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20210120 N/A ANDA ANDA214603 XLCare Pharmaceuticals, Inc. GEMFIBROZIL 600 mg/1 60 TABLET in 1 BOTTLE (72865-186-60)
71335-1996-1 71335-1996 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20220210 N/A ANDA ANDA214603 Bryant Ranch Prepack GEMFIBROZIL 600 mg/1 60 TABLET in 1 BOTTLE (71335-1996-1)
71335-1996-2 71335-1996 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20220210 N/A ANDA ANDA214603 Bryant Ranch Prepack GEMFIBROZIL 600 mg/1 30 TABLET in 1 BOTTLE (71335-1996-2)
71335-1996-3 71335-1996 HUMAN PRESCRIPTION DRUG GEMFIBROZIL Gemfibrozil TABLET ORAL 20220210 N/A ANDA ANDA214603 Bryant Ranch Prepack GEMFIBROZIL 600 mg/1 100 TABLET in 1 BOTTLE (71335-1996-3)
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