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 90 条，共 5 页，当前第 4 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
68382-018-01 68382-018 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (68382-018-01)
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)
68382-018-10 68382-018 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (68382-018-10)
68382-018-14 68382-018 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (68382-018-14)
68382-018-16 68382-018 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (68382-018-16)
68382-019-01 68382-019 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (68382-019-01)
68382-019-05 68382-019 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 500 TABLET in 1 BOTTLE (68382-019-05)
68382-019-06 68382-019 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (68382-019-06)
68382-019-10 68382-019 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 TABLET in 1 BOTTLE (68382-019-10)
68382-019-14 68382-019 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 TABLET in 1 BOTTLE (68382-019-14)
68382-019-16 68382-019 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (68382-019-16)
68382-020-01 68382-020 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (68382-020-01)
68382-020-05 68382-020 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 500 TABLET in 1 BOTTLE (68382-020-05)
68382-020-06 68382-020 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (68382-020-06)
68382-020-10 68382-020 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (68382-020-10)
68382-020-14 68382-020 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 60 TABLET in 1 BOTTLE (68382-020-14)
68382-020-16 68382-020 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (68382-020-16)
68382-021-01 68382-021 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (68382-021-01)
68382-021-05 68382-021 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 500 TABLET in 1 BOTTLE (68382-021-05)
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