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 3 页 ，可点击列名称排序
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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
70710-1700-5 70710-1700 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-5)
70710-1700-9 70710-1700 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-9)
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)
70710-1698-5 70710-1698 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-5)
70710-1698-9 70710-1698 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-9)
68788-8774-8 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/1 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-8)
68071-4442-9 68071-4442 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20180521 N/A ANDA ANDA090174 NuCare Pharmaceuticals,Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4442-9)
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)
68788-8774-9 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 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-9)
68382-036-06 68382-036 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-06)
68382-036-10 68382-036 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-10)
68382-036-16 68382-036 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-16)
50090-6301-0 50090-6301 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20221229 N/A ANDA ANDA090174 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 33 BLISTER PACK in 1 CARTON (50090-6301-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
68788-6806-1 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/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-1)
68788-6806-2 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 20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-2)
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