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=ANDA214127"
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
67877-726-30 67877-726 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-30)
67877-726-90 67877-726 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-90)
67877-727-30 67877-727 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-727-30)
67877-727-90 67877-727 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-727-90)
67877-729-30 67877-729 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 225 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-729-30)
67877-729-90 67877-729 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 225 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-729-90)
67877-728-30 67877-728 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-728-30)
67877-728-90 67877-728 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20210611 N/A ANDA ANDA214127 Ascend Laboratories, LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-728-90)
70518-3820-0 70518-3820 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET, EXTENDED RELEASE ORAL 20230803 N/A ANDA ANDA214127 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3820-0)
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