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
0904-7488-61 0904-7488 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20251008 N/A ANDA ANDA200834 Major Pharmaceuticals VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 BLISTER PACK in 1 CARTON (0904-7488-61) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
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)
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)
42708-194-30 42708-194 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20260201 N/A ANDA ANDA200834 QPharma, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42708-194-30)
50090-7941-1 50090-7941 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20260318 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7941-1)
50090-7941-2 50090-7941 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20260318 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7941-2)
50090-2519-0 50090-2519 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20161109 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2519-0)
50090-2519-1 50090-2519 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20161017 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2519-1)
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)
68788-8752-9 68788-8752 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241014 N/A ANDA ANDA200834 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8752-9)
50090-7942-0 50090-7942 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20260318 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7942-0)
50090-7942-1 50090-7942 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20260318 N/A ANDA ANDA200834 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7942-1)
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