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
71335-1642-1 71335-1642 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20200616 N/A ANDA ANDA200834 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1642-1)
71335-1642-2 71335-1642 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20200608 N/A ANDA ANDA200834 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 150 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1642-2)
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)
71205-408-60 71205-408 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20200221 N/A ANDA ANDA200834 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-408-60)
71205-408-90 71205-408 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20200221 N/A ANDA ANDA200834 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-408-90)
82804-038-30 82804-038 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231107 N/A ANDA ANDA200834 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-30)
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)
65862-527-90 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)
50090-2180-0 50090-2180 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20151026 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-0)
50090-2180-1 50090-2180 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20151026 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-1)
76420-630-01 76420-630 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase