| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 67877-549-30 | 67877-549 | HUMAN PRESCRIPTION DRUG | Deferasirox | Deferasirox | TABLET, FOR SUSPENSION | ORAL | 20191122 | N/A | ANDA | ANDA210519 | Ascend Laboratories, LLC | DEFERASIROX | 125 mg/1 | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (67877-549-30) |
| 67877-550-30 | 67877-550 | HUMAN PRESCRIPTION DRUG | Deferasirox | Deferasirox | TABLET, FOR SUSPENSION | ORAL | 20191122 | N/A | ANDA | ANDA210519 | Ascend Laboratories, LLC | DEFERASIROX | 250 mg/1 | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (67877-550-30) |
| 67877-551-30 | 67877-551 | HUMAN PRESCRIPTION DRUG | Deferasirox | Deferasirox | TABLET, FOR SUSPENSION | ORAL | 20191122 | N/A | ANDA | ANDA210519 | Ascend Laboratories, LLC | DEFERASIROX | 500 mg/1 | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (67877-551-30) |