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=ANDA077653"
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
65841-671-01 65841-671 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (65841-671-01)
65841-671-05 65841-671 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 25 mg/1 500 TABLET in 1 BOTTLE (65841-671-05)
65841-671-06 65841-671 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (65841-671-06)
65841-671-10 65841-671 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (65841-671-10)
65841-671-14 65841-671 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (65841-671-14)
65841-671-16 65841-671 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (65841-671-16)
65841-675-01 65841-675 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (65841-675-01)
65841-675-05 65841-675 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 500 TABLET in 1 BOTTLE (65841-675-05)
60760-728-60 60760-728 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20230421 N/A ANDA ANDA077653 ST. MARY'S MEDICAL PARK PHARMACY VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-728-60)
65841-674-01 65841-674 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (65841-674-01)
65841-674-05 65841-674 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 500 TABLET in 1 BOTTLE (65841-674-05)
65841-674-06 65841-674 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (65841-674-06)
65841-674-10 65841-674 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 1000 TABLET in 1 BOTTLE (65841-674-10)
65841-674-14 65841-674 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 TABLET in 1 BOTTLE (65841-674-14)
65841-674-16 65841-674 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (65841-674-16)
68001-158-00 68001-158 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20131125 N/A ANDA ANDA077653 BluePoint Laboratories VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (68001-158-00)
68071-3431-0 68071-3431 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20230727 N/A ANDA ANDA077653 NuCare Pharmaceuticals,Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (68071-3431-0)
65841-672-01 65841-672 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (65841-672-01)
65841-672-05 65841-672 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 500 TABLET in 1 BOTTLE (65841-672-05)
65841-672-06 65841-672 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (65841-672-06)
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