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=NDA216993"
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
65597-504-04 65597-504 HUMAN PRESCRIPTION DRUG VANFLYTA QUIZARTINIB TABLET, FILM COATED ORAL 20230720 N/A NDA NDA216993 Daiichi Sankyo Inc. QUIZARTINIB DIHYDROCHLORIDE 17.7 mg/1 1 BOTTLE in 1 CARTON (65597-504-04) / 14 TABLET, FILM COATED in 1 BOTTLE
65597-504-28 65597-504 HUMAN PRESCRIPTION DRUG VANFLYTA QUIZARTINIB TABLET, FILM COATED ORAL 20230720 N/A NDA NDA216993 Daiichi Sankyo Inc. QUIZARTINIB DIHYDROCHLORIDE 17.7 mg/1 1 BOTTLE in 1 CARTON (65597-504-28) / 28 TABLET, FILM COATED in 1 BOTTLE
65597-511-04 65597-511 HUMAN PRESCRIPTION DRUG VANFLYTA QUIZARTINIB TABLET, FILM COATED ORAL 20230720 N/A NDA NDA216993 Daiichi Sankyo Inc. QUIZARTINIB DIHYDROCHLORIDE 26.5 mg/1 1 BOTTLE in 1 CARTON (65597-511-04) / 14 TABLET, FILM COATED in 1 BOTTLE
65597-511-28 65597-511 HUMAN PRESCRIPTION DRUG VANFLYTA QUIZARTINIB TABLET, FILM COATED ORAL 20230720 N/A NDA NDA216993 Daiichi Sankyo Inc. QUIZARTINIB DIHYDROCHLORIDE 26.5 mg/1 1 BOTTLE in 1 CARTON (65597-511-28) / 28 TABLET, FILM COATED in 1 BOTTLE
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