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"
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
70710-1700-4 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 10 BLISTER PACK in 1 CARTON (70710-1700-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1700-2)
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)
68382-036-06 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)
68382-035-16 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 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-035-16)
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