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 152 条，共 8 页，当前第 3 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
68788-9265-6 68788-9265 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20141203 N/A ANDA ANDA077614 Preferred Pharmaceuticals,Inc. CARVEDILOL 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-9265-6)
68788-9265-9 68788-9265 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20141203 N/A ANDA ANDA077614 Preferred Pharmaceuticals,Inc. CARVEDILOL 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-9265-9)
68382-093-01 68382-093 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-093-01)
68071-2230-3 68071-2230 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20250102 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 12.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-3)
68071-2230-6 68071-2230 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20200804 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 12.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-2230-6)
68071-2230-8 68071-2230 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20200804 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 12.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-8)
68382-093-05 68382-093 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-093-05)
68382-093-17 68382-093 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 6.25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68382-093-17)
68071-4956-6 68071-4956 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20190703 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-4956-6)
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)
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)
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)
51655-030-83 51655-030 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220413 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 12.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-83)
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