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
63187-414-30 63187-414 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20190101 N/A ANDA ANDA077653 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (63187-414-30)
63187-414-60 63187-414 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20190101 N/A ANDA ANDA077653 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 TABLET in 1 BOTTLE (63187-414-60)
68084-844-01 68084-844 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20150513 N/A ANDA ANDA077653 American Health Packaging VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-844-01) / 1 TABLET in 1 BLISTER PACK (68084-844-11)
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)
50090-2408-0 50090-2408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20160519 N/A ANDA ANDA077653 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (50090-2408-0)
50090-2408-1 50090-2408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20160519 N/A ANDA ANDA077653 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (50090-2408-1)
68084-856-01 68084-856 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20150306 N/A ANDA ANDA077653 American Health Packaging VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01) / 1 TABLET in 1 BLISTER PACK (68084-856-11)
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)
63629-3324-3 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20100203 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (63629-3324-3)
63629-3324-4 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20120202 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 28 TABLET in 1 BOTTLE (63629-3324-4)
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