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=NDA216951"
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
0173-0897-13 0173-0897 HUMAN PRESCRIPTION DRUG Jesduvroq daprodustat TABLET, FILM COATED ORAL 20230201 N/A NDA NDA216951 GlaxoSmithKline LLC DAPRODUSTAT 1 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0173-0897-13)
0173-0903-13 0173-0903 HUMAN PRESCRIPTION DRUG Jesduvroq daprodustat TABLET, FILM COATED ORAL 20230201 N/A NDA NDA216951 GlaxoSmithKline LLC DAPRODUSTAT 2 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0173-0903-13)
0173-0906-13 0173-0906 HUMAN PRESCRIPTION DRUG Jesduvroq daprodustat TABLET, FILM COATED ORAL 20230201 N/A NDA NDA216951 GlaxoSmithKline LLC DAPRODUSTAT 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0173-0906-13)
0173-0911-13 0173-0911 HUMAN PRESCRIPTION DRUG Jesduvroq daprodustat TABLET, FILM COATED ORAL 20230201 N/A NDA NDA216951 GlaxoSmithKline LLC DAPRODUSTAT 6 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0173-0911-13)
0173-0914-13 0173-0914 HUMAN PRESCRIPTION DRUG Jesduvroq daprodustat TABLET, FILM COATED ORAL 20230201 N/A NDA NDA216951 GlaxoSmithKline LLC DAPRODUSTAT 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0173-0914-13)
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