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=ANDA220250"
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
72205-158-30 72205-158 HUMAN PRESCRIPTION DRUG eltrombopag eltrombopag olamine TABLET, FILM COATED ORAL 20260114 N/A ANDA ANDA220250 Novadoz Pharmaceuticals LLC ELTROMBOPAG OLAMINE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-158-30)
72205-158-19 72205-158 HUMAN PRESCRIPTION DRUG eltrombopag eltrombopag olamine TABLET, FILM COATED ORAL 20260114 N/A ANDA ANDA220250 Novadoz Pharmaceuticals LLC ELTROMBOPAG OLAMINE 50 mg/1 19 TABLET, FILM COATED in 1 BOTTLE (72205-158-19)
72205-157-30 72205-157 HUMAN PRESCRIPTION DRUG eltrombopag eltrombopag olamine TABLET, FILM COATED ORAL 20260114 N/A ANDA ANDA220250 Novadoz Pharmaceuticals LLC ELTROMBOPAG OLAMINE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-157-30)
72205-156-30 72205-156 HUMAN PRESCRIPTION DRUG eltrombopag eltrombopag olamine TABLET, FILM COATED ORAL 20260114 N/A ANDA ANDA220250 Novadoz Pharmaceuticals LLC ELTROMBOPAG OLAMINE 12.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-156-30)
72205-159-30 72205-159 HUMAN PRESCRIPTION DRUG eltrombopag eltrombopag olamine TABLET, FILM COATED ORAL 20260114 N/A ANDA ANDA220250 Novadoz Pharmaceuticals LLC ELTROMBOPAG OLAMINE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-159-30)
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