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
68788-8140-9 68788-8140 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20220211 N/A ANDA ANDA200834 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-9)
71205-369-90 71205-369 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20191203 N/A ANDA ANDA200834 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-369-90)
76420-632-60 76420-632 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-632-60)
76420-632-90 76420-632 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20231018 N/A ANDA ANDA200834 Asclemed USA, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-632-90)
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