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=ANDA212884"
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
60219-1417-3 60219-1417 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 12.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60219-1417-3)
60219-1416-3 60219-1416 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-1416-3)
60219-1415-3 60219-1415 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60219-1415-3)
60219-1414-3 60219-1414 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60219-1414-3)
69238-1414-3 69238-1414 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69238-1414-3)
69238-1415-3 69238-1415 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69238-1415-3)
69238-1416-3 69238-1416 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69238-1416-3)
69238-1417-3 69238-1417 HUMAN PRESCRIPTION DRUG Eltrombopag Olamine Eltrombopag TABLET, FILM COATED ORAL 20260115 N/A ANDA ANDA212884 Amneal Pharmaceuticals NY LLC ELTROMBOPAG OLAMINE 12.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69238-1417-3)
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