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=ANDA211593"
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
47781-381-30 47781-381 HUMAN PRESCRIPTION DRUG Pregabalin Extended Release PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210414 N/A ANDA ANDA211593 Alvogen Inc. PREGABALIN 330 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-381-30)
47781-380-30 47781-380 HUMAN PRESCRIPTION DRUG Pregabalin Extended Release PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210414 N/A ANDA ANDA211593 Alvogen Inc. PREGABALIN 165 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-380-30)
47781-379-30 47781-379 HUMAN PRESCRIPTION DRUG Pregabalin Extended Release PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210414 N/A ANDA ANDA211593 Alvogen Inc. PREGABALIN 82.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-379-30)
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