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
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)
68382-036-10 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)
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)
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)
65841-752-06 65841-752 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-752-06)
65841-752-10 65841-752 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-752-10)
65841-752-16 65841-752 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-752-16)
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)
70771-1837-5 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-5)
70771-1837-9 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-9)
68382-035-06 68382-035 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-035-06)
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)
65841-753-06 65841-753 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-06)
65841-753-10 65841-753 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-10)
65841-753-16 65841-753 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-16)
68382-035-10 68382-035 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-035-10)
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)
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