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 3 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
70518-2652-2 70518-2652 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20201223 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-2652-2)
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)
57237-172-01 57237-172 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (57237-172-01)
57237-172-90 57237-172 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (57237-172-90)
57237-176-01 57237-176 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (57237-176-01)
57237-176-90 57237-176 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (57237-176-90)
65862-406-01 65862-406 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (65862-406-01)
65862-406-10 65862-406 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 10 BLISTER PACK in 1 CARTON (65862-406-10) / 10 TABLET in 1 BLISTER PACK
65862-406-30 65862-406 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (65862-406-30)
65862-406-59 65862-406 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 5000 TABLET in 1 BOTTLE (65862-406-59)
65862-406-90 65862-406 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (65862-406-90)
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)
60760-187-60 60760-187 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20190529 N/A ANDA ANDA090555 St. Mary's Medical Park Pharmacy VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60)
60760-304-30 60760-304 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200616 N/A ANDA ANDA090555 St. Mary's Medical Park Pharmacy VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30)
70518-2659-0 70518-2659 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200327 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BLISTER PACK (70518-2659-0)
65862-406-99 65862-406 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (65862-406-99)
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