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=ANDA200834"
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
82009-058-05 82009-058 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20221121 N/A ANDA ANDA200834 QUALLENT PHARMACEUTICALS HEALTH LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-058-05)
68084-698-01 68084-698 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140206 N/A ANDA ANDA200834 American Health Packaging VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-698-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-698-11)
71335-1993-3 71335-1993 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20211118 N/A ANDA ANDA200834 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1993-3)
71335-1993-4 71335-1993 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20240405 N/A ANDA ANDA200834 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1993-4)
71335-1993-5 71335-1993 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20240405 N/A ANDA ANDA200834 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1993-5)
65862-527-01 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-01)
65862-527-10 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 10 BLISTER PACK in 1 CARTON (65862-527-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
65862-527-30 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-30)
65862-527-47 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-47)
65862-527-59 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 5000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-59)
65862-527-90 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-90)
65862-527-99 65862-527 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-99)
65862-697-01 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-01)
65862-697-05 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-05)
65862-697-10 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 10 BLISTER PACK in 1 CARTON (65862-697-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
65862-697-26 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 2500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-26)
65862-697-30 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-30)
65862-697-47 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-47)
65862-697-90 65862-697 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20111123 N/A ANDA ANDA200834 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-90)
72189-363-30 72189-363 HUMAN PRESCRIPTION DRUG Venlafaxine HCL ER Venlafaxine HCL ER CAPSULE, EXTENDED RELEASE ORAL 20220826 N/A ANDA ANDA200834 Direct_Rx VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase