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"
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
50090-4853-0 50090-4853 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200120 N/A ANDA ANDA090555 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (50090-4853-0)
50090-4853-1 50090-4853 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200120 N/A ANDA ANDA090555 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (50090-4853-1)
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)
57237-173-90 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 90 TABLET in 1 BOTTLE (57237-173-90)
71335-1104-1 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20190220 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 TABLET in 1 BOTTLE (71335-1104-1)
71335-1104-2 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20190213 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (71335-1104-2)
71335-1104-3 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200103 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (71335-1104-3)
71335-1104-4 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20211228 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 28 TABLET in 1 BOTTLE (71335-1104-4)
71335-1104-5 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20211228 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 120 TABLET in 1 BOTTLE (71335-1104-5)
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)
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)
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)
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