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=ANDA077614"
符合检索条件的记录共 147 条，共 8 页，当前第 2 页 ，可点击列名称排序
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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
71335-2101-1 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2101-1)
71335-2101-2 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220714 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2101-2)
71335-2101-3 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220721 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2101-3)
71335-2101-4 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20231117 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-2101-4)
71335-2101-5 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2101-5)
71335-2101-6 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220708 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2101-6)
71335-2101-7 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 25 TABLET, FILM COATED in 1 BOTTLE (71335-2101-7)
71335-2101-8 71335-2101 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 6.25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-2101-8)
68071-3138-3 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3138-3)
68071-3138-6 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3138-6)
68071-3138-8 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-3138-8)
68071-3138-9 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3138-9)
50090-6742-0 50090-6742 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20231013 N/A ANDA ANDA077614 A-S Medication Solutions CARVEDILOL 6.25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6742-0)
50090-6742-1 50090-6742 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20231013 N/A ANDA ANDA077614 A-S Medication Solutions CARVEDILOL 6.25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-6742-1)
50090-6742-3 50090-6742 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20231013 N/A ANDA ANDA077614 A-S Medication Solutions CARVEDILOL 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6742-3)
50090-6742-4 50090-6742 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20231013 N/A ANDA ANDA077614 A-S Medication Solutions CARVEDILOL 6.25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6742-4)
50090-6878-0 50090-6878 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20231205 N/A ANDA ANDA077614 A-S Medication Solutions CARVEDILOL 12.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6878-0)
68382-092-01 68382-092 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 3.125 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-092-01)
68382-092-05 68382-092 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 3.125 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-092-05)
68382-092-17 68382-092 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 3.125 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68382-092-17)
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