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 5 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
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)
51655-034-25 51655-034 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20221018 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 3.125 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-25)
51655-034-52 51655-034 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220809 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 3.125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-52)
51655-034-83 51655-034 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20230111 N/A ANDA ANDA077614 Northwind Pharmaceuticals, LLC CARVEDILOL 3.125 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-83)
51655-397-25 51655-397 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077614 Northwind Pharmaceuticals CARVEDILOL 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-25)
51655-397-26 51655-397 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20200708 N/A ANDA ANDA077614 Northwind Pharmaceuticals CARVEDILOL 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-26)
51655-397-52 51655-397 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077614 Northwind Pharmaceuticals CARVEDILOL 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-52)
51655-397-83 51655-397 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA077614 Northwind Pharmaceuticals CARVEDILOL 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-83)
63187-424-60 63187-424 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077614 Proficient Rx LP CARVEDILOL 6.25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-424-60)
63187-570-30 63187-570 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077614 Proficient Rx LP CARVEDILOL 3.125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-570-30)
63187-570-60 63187-570 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077614 Proficient Rx LP CARVEDILOL 3.125 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-570-60)
63187-570-90 63187-570 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077614 Proficient Rx LP CARVEDILOL 3.125 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-570-90)
63629-4060-1 63629-4060 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20090827 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 3.125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63629-4060-1)
63629-4060-2 63629-4060 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20090904 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 3.125 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-4060-2)
63629-4060-3 63629-4060 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20151124 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 3.125 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (63629-4060-3)
63629-4060-4 63629-4060 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20110502 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 3.125 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63629-4060-4)
63629-4060-5 63629-4060 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20140530 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 3.125 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-4060-5)
63629-4060-6 63629-4060 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20141028 N/A ANDA ANDA077614 Bryant Ranch Prepack CARVEDILOL 3.125 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (63629-4060-6)
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)
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