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=ANDA090174"
符合检索条件的记录共 67 条，共 4 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
68788-6806-8 68788-6806 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20161107 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-8)
68788-6806-9 68788-6806 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20161107 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-9)
68382-034-06 68382-034 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-06)
68382-034-10 68382-034 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10)
68382-034-16 68382-034 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-16)
65841-751-06 65841-751 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-06)
65841-751-10 65841-751 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-10)
65841-751-16 65841-751 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-16)
70771-1836-0 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-0)
70771-1836-3 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-3)
70771-1836-4 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 10 BLISTER PACK in 1 CARTON (70771-1836-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1836-2)
70771-1836-5 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-5)
70771-1836-9 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-9)
70710-1699-0 70710-1699 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1699-0)
70710-1699-3 70710-1699 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1699-3)
70710-1699-4 70710-1699 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 CARTON (70710-1699-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1699-2)
68788-8774-1 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-1)
68788-8774-2 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-2)
68788-8774-3 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-3)
68788-8774-6 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-6)
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