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
68071-3886-3 68071-3886 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250819 N/A ANDA ANDA200834 NuCare Pharmaceuticals, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3886-3)
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)
70518-2259-1 70518-2259 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20200819 N/A ANDA ANDA200834 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2259-1)
70518-2259-2 70518-2259 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA200834 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2259-2)
70518-2259-5 70518-2259 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230828 N/A ANDA ANDA200834 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 POUCH in 1 BOX (70518-2259-5) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2259-6)
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)
72189-363-60 72189-363 HUMAN PRESCRIPTION DRUG Venlafaxine HCL ER Venlafaxine HCL ER CAPSULE, EXTENDED RELEASE ORAL 20220622 N/A ANDA ANDA200834 Direct_Rx VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-60)
60760-836-30 60760-836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250513 N/A ANDA ANDA200834 ST. MARY'S MEDICAL PARK PHARMACY VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-836-30)
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)
82804-038-60 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 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-60)
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)
76420-632-01 76420-632 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-632-01)
76420-632-15 76420-632 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-632-15)
76420-632-30 76420-632 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-632-30)
76420-632-60 76420-632 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-632-60)
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