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=ANDA203828"
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
50090-5775-2 50090-5775 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211007 N/A ANDA ANDA203828 A-S Medication Solutions NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (50090-5775-2)
67877-393-01 67877-393 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210916 N/A ANDA ANDA203828 Ascend Laboratories, LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (67877-393-01)
67877-393-30 67877-393 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210916 N/A ANDA ANDA203828 Ascend Laboratories, LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (67877-393-30)
67877-393-33 67877-393 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210916 N/A ANDA ANDA203828 Ascend Laboratories, LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 1 BLISTER PACK in 1 CARTON (67877-393-33) / 10 TABLET in 1 BLISTER PACK
67877-393-90 67877-393 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210916 N/A ANDA ANDA203828 Ascend Laboratories, LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (67877-393-90)
50090-5708-0 50090-5708 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210923 N/A ANDA ANDA203828 A-S Medication Solutions NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 5 TABLET in 1 BOTTLE (50090-5708-0)
50090-5708-1 50090-5708 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211007 N/A ANDA ANDA203828 A-S Medication Solutions NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (50090-5708-1)
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