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=ANDA205468"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
69367-418-30 69367-418 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20251118 N/A ANDA ANDA205468 Westminster Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 225 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-418-30)
69367-418-09 69367-418 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20251118 N/A ANDA ANDA205468 Westminster Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 225 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-418-09)
69367-417-30 69367-417 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20251118 N/A ANDA ANDA205468 Westminster Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30)
69367-417-09 69367-417 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20251118 N/A ANDA ANDA205468 Westminster Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09)
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