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=ANDA213239"
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
0054-0711-19 0054-0711 HUMAN PRESCRIPTION DRUG Deferiprone Deferiprone TABLET, COATED ORAL 20220208 N/A ANDA ANDA213239 Hikma Pharmaceuticals USA Inc. DEFERIPRONE 1000 mg/1 50 TABLET, COATED in 1 BOTTLE (0054-0711-19)
0054-0711-23 0054-0711 HUMAN PRESCRIPTION DRUG Deferiprone Deferiprone TABLET, COATED ORAL 20220208 N/A ANDA ANDA213239 Hikma Pharmaceuticals USA Inc. DEFERIPRONE 1000 mg/1 150 TABLET, COATED in 1 BOTTLE (0054-0711-23)
0054-0711-28 0054-0711 HUMAN PRESCRIPTION DRUG Deferiprone Deferiprone TABLET, COATED ORAL 20220208 N/A ANDA ANDA213239 Hikma Pharmaceuticals USA Inc. DEFERIPRONE 1000 mg/1 300 TABLET, COATED in 1 BOTTLE (0054-0711-28)
0054-0576-25 0054-0576 HUMAN PRESCRIPTION DRUG Deferiprone Deferiprone TABLET, COATED ORAL 20210603 N/A ANDA ANDA213239 Hikma Pharmaceuticals USA Inc. DEFERIPRONE 500 mg/1 100 TABLET, COATED in 1 BOTTLE (0054-0576-25)
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