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=ANDA076690"
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
70518-3219-0 70518-3219 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20210913 N/A ANDA ANDA076690 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BLISTER PACK (70518-3219-0)
0093-9157-01 0093-9157 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20060804 N/A ANDA ANDA076690 Teva Pharmaceuticals USA, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (0093-9157-01)
0093-9163-01 0093-9163 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20060804 N/A ANDA ANDA076690 Teva Pharmaceuticals USA, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (0093-9163-01)
0093-9149-01 0093-9149 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20060804 N/A ANDA ANDA076690 Teva Pharmaceuticals USA, Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (0093-9149-01)
0093-9148-01 0093-9148 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20060804 N/A ANDA ANDA076690 Teva Pharmaceuticals USA, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (0093-9148-01)
0093-9147-01 0093-9147 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20060804 N/A ANDA ANDA076690 Teva Pharmaceuticals USA, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (0093-9147-01)
0615-8346-39 0615-8346 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET ORAL 20200722 N/A ANDA ANDA076690 NCS HealthCare of KY, LLC dba Vangard Labs VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BLISTER PACK (0615-8346-39)
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