| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NITROPRESS | 018450 | 001 | NDA | SODIUM NITROPRUSSIDE | INJECTABLE;INJECTION | 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 1981/09/08 | Approved Prior to Jan 1, 1982 | ABBVIE | Discontinued |
| NITROPRESS | 070566 | 001 | ANDA | SODIUM NITROPRUSSIDE | INJECTABLE;INJECTION | 50MG/VIAL | No | No | 1986/06/09 | 1986/06/09 | HOSPIRA | Discontinued |
| NITROPRESS | 071555 | 001 | ANDA | SODIUM NITROPRUSSIDE | INJECTABLE;INJECTION | 50MG/VIAL | No | No | 1987/11/16 | 1987/11/16 | ABBOTT | Discontinued |
| NITROPRESS | 071961 | 001 | ANDA | SODIUM NITROPRUSSIDE | INJECTABLE;INJECTION | 25MG/ML | No | No | 1988/08/01 | 1988/08/01 | VPNA | Discontinued |