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=ANDA090555"
符合检索条件的记录共 68 条，共 4 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
65862-405-01 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (65862-405-01)
65862-405-10 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 10 BLISTER PACK in 1 CARTON (65862-405-10) / 10 TABLET in 1 BLISTER PACK
65862-405-30 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (65862-405-30)
65862-405-60 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 TABLET in 1 BOTTLE (65862-405-60)
65862-405-66 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 6000 TABLET in 1 BOTTLE (65862-405-66)
65862-405-90 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (65862-405-90)
65862-405-99 65862-405 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 TABLET in 1 BOTTLE (65862-405-99)
65862-408-01 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (65862-408-01)
65862-408-10 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 10 BLISTER PACK in 1 CARTON (65862-408-10) / 10 TABLET in 1 BLISTER PACK
70518-1385-0 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20180824 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1385-0)
70518-1385-1 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20181004 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-1385-1)
70518-1385-3 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20231107 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-1385-3)
51655-223-26 51655-223 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20230227 N/A ANDA ANDA090555 Northwind Health Company, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-223-26)
51655-223-52 51655-223 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20221025 N/A ANDA ANDA090555 Northwind Health Company, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-223-52)
51655-323-52 51655-323 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20230502 N/A ANDA ANDA090555 Northwind Health Company, LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52)
65862-408-20 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 20 TABLET in 1 BOTTLE (65862-408-20)
65862-408-66 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 6000 TABLET in 1 BOTTLE (65862-408-66)
65862-408-90 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (65862-408-90)
65862-408-99 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 1000 TABLET in 1 BOTTLE (65862-408-99)
57237-173-01 57237-173 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (57237-173-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase