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
65841-673-06 65841-673 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (65841-673-06)
65841-673-10 65841-673 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (65841-673-10)
65841-673-14 65841-673 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 60 TABLET in 1 BOTTLE (65841-673-14)
65841-673-16 65841-673 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (65841-673-16)
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)
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)
65841-675-06 65841-675 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (65841-675-06)
65841-675-10 65841-675 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 1000 TABLET in 1 BOTTLE (65841-675-10)
65841-675-14 65841-675 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 60 TABLET in 1 BOTTLE (65841-675-14)
65841-675-16 65841-675 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (65841-675-16)
60760-121-30 60760-121 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20110130 N/A ANDA ANDA077653 St. Marys Medical Park Pharmacy VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30)
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)
68084-844-01 68084-844 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20150417 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)
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)
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