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=ANDA212277"
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
31722-003-01 31722-003 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190708 N/A ANDA ANDA212277 Camber Pharmaceuticals, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 CARTON (31722-003-01) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
31722-003-05 31722-003 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190708 N/A ANDA ANDA212277 Camber Pharmaceuticals, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-05)
31722-003-30 31722-003 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190708 N/A ANDA ANDA212277 Camber Pharmaceuticals, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-30)
31722-003-90 31722-003 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20190708 N/A ANDA ANDA212277 Camber Pharmaceuticals, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase