| 商品名 | 申请号 | 产品号 | 申请类型 | 活性成分 | 剂型/给药途径 | 规格/剂量 | RLD | RS | 申请号原始批准/暂定批准日期 | 产品号批准日期 | 申请人 | 市场状态 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| RISEDRONATE SODIUM | 203533 | 003 | ANDA | RISEDRONATE SODIUM | TABLET;ORAL | 35MG | No | No | 2016/11/29 | 2016/11/29 | MACLEODS PHARMS LTD | Prescription |
| RISEDRONATE SODIUM | 205066 | 001 | ANDA | RISEDRONATE SODIUM | TABLET, DELAYED RELEASE;ORAL | 35MG | No | No | 2018/06/29 | 2018/06/29 | IMPAX LABS INC | Discontinued |
| RISEDRONATE SODIUM | 203822 | 001 | ANDA | RISEDRONATE SODIUM | TABLET, DELAYED RELEASE;ORAL | 35MG | No | No | 2018/09/11 | 2018/09/11 | ZYDUS PHARMS | Discontinued |
| RISEDRONATE SODIUM | 207516 | 001 | ANDA | RISEDRONATE SODIUM | TABLET;ORAL | 35MG | No | No | 2019/02/15 | 2019/02/15 | HANGZHOU BINJIANG | Discontinued |
| RISEDRONATE SODIUM | 205280 | 001 | ANDA | RISEDRONATE SODIUM | TABLET;ORAL | 30MG | No | No | 2019/05/13 | 2019/05/13 | ORBION PHARMS | Prescription |
| RISEDRONATE SODIUM | 205280 | 002 | ANDA | RISEDRONATE SODIUM | TABLET;ORAL | 35MG | No | No | 2019/05/13 | 2019/05/13 | ORBION PHARMS | Prescription |
| RISEDRONATE SODIUM | 203925 | 001 | ANDA | RISEDRONATE SODIUM | TABLET, DELAYED RELEASE;ORAL | 35MG | No | No | 2019/07/09 | 2019/07/09 | SUN PHARM | Prescription |