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"
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
65841-619-05 65841-619 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-619-05)
65841-619-17 65841-619 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (65841-619-17)
70518-4389-0 70518-4389 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20250708 N/A ANDA ANDA077614 REMEDYREPACK INC. CARVEDILOL 12.5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4389-0)
70518-4389-1 70518-4389 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20250819 N/A ANDA ANDA077614 REMEDYREPACK INC. CARVEDILOL 12.5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4389-1)
68001-151-03 68001-151 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20140422 N/A ANDA ANDA077614 BluePoint Laboratories CARVEDILOL 12.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68001-151-03)
71335-1545-1 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20100330 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1545-1)
71335-1545-2 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20100330 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1545-2)
71335-1545-3 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20100330 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1545-3)
71335-1545-4 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20100330 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1545-4)
71335-1545-5 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20100330 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1545-5)
71335-1545-6 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20100330 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-1545-6)
71335-1545-7 71335-1545 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20240430 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 12.5 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-1545-7)
68071-2780-8 68071-2780 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220705 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 6.25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-2780-8)
68071-2780-9 68071-2780 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220705 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 6.25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2780-9)
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)
51655-030-25 51655-030 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220413 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 12.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-25)
51655-030-26 51655-030 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220714 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 12.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-26)
51655-030-52 51655-030 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220323 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 12.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-52)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase