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 5 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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 Health Company, 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 Health Company, 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 Health Company, 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 Health Company, 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 Health Company, LLC 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 Health Company, LLC 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 Health Company, LLC 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 Health Company, LLC CARVEDILOL 25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-83)
60760-494-60 60760-494 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20190604 N/A ANDA ANDA077614 St. Mary's Medical Park Pharmacy CARVEDILOL 12.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-494-60)
60760-582-60 60760-582 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20221017 N/A ANDA ANDA077614 ST. MARY'S MEDICAL PARK PHARMACY CARVEDILOL 6.25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-582-60)
65841-616-01 65841-616 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 3.125 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-616-01)
65841-616-05 65841-616 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 3.125 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-616-05)
65841-616-17 65841-616 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 3.125 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (65841-616-17)
65841-617-01 65841-617 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-617-01)
65841-617-05 65841-617 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-617-05)
65841-617-17 65841-617 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 6.25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (65841-617-17)
65841-618-01 65841-618 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 12.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-618-01)
65841-618-05 65841-618 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 12.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-618-05)
65841-618-17 65841-618 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 12.5 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (65841-618-17)
65841-619-01 65841-619 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Lifesciences Limited CARVEDILOL 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-619-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase