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"
符合检索条件的记录共 93 条，共 5 页，当前第 2 页 ，可点击列名称排序
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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
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)
65841-671-05 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)
68382-018-05 68382-018 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 500 TABLET in 1 BOTTLE (68382-018-05)
68382-018-06 68382-018 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (68382-018-06)
71335-2709-1 71335-2709 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20250926 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (71335-2709-1)
71335-2709-2 71335-2709 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20250926 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 100 mg/1 60 TABLET in 1 BOTTLE (71335-2709-2)
71335-2709-3 71335-2709 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20250926 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (71335-2709-3)
71335-2709-4 71335-2709 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20250926 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 100 mg/1 18 TABLET in 1 BOTTLE (71335-2709-4)
68084-896-25 68084-896 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20150929 N/A ANDA ANDA077653 American Health Packaging VENLAFAXINE HYDROCHLORIDE 25 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-896-25) / 1 TABLET in 1 BLISTER PACK (68084-896-95)
65841-673-01 65841-673 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (65841-673-01)
65841-673-05 65841-673 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 500 TABLET in 1 BOTTLE (65841-673-05)
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)
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