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=ANDA208717"
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
72241-033-22 72241-033 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (72241-033-22)
72241-034-04 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (72241-034-04)
72241-034-05 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (72241-034-05)
72241-034-11 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (72241-034-11)
72241-034-22 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (72241-034-22)
72241-035-04 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (72241-035-04)
72241-035-05 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (72241-035-05)
72241-035-11 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 1000 TABLET in 1 BOTTLE (72241-035-11)
72241-035-22 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (72241-035-22)
72241-032-05 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (72241-032-05)
72241-032-11 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 1000 TABLET in 1 BOTTLE (72241-032-11)
72241-032-22 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (72241-032-22)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase