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=ANDA206252"
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
68071-3463-6 68071-3463 HUMAN PRESCRIPTION DRUG QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET, EXTENDED RELEASE ORAL 20230719 N/A ANDA ANDA206252 NuCare Pharmaceuticals,Inc. QUETIAPINE FUMARATE 50 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3463-6)
68001-511-06 68001-511 HUMAN PRESCRIPTION DRUG QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET, EXTENDED RELEASE ORAL 20210831 N/A ANDA ANDA206252 Bluepoint Laboratories QUETIAPINE FUMARATE 50 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-511-06)
16729-132-12 16729-132 HUMAN PRESCRIPTION DRUG QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET, EXTENDED RELEASE ORAL 20171130 N/A ANDA ANDA206252 Accord Healthcare Inc. QUETIAPINE FUMARATE 50 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-132-12)
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