| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NORFLEX | 012157 | 001 | NDA | ORPHENADRINE CITRATE | TABLET, EXTENDED RELEASE;ORAL | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 1959/11/04 | Approved Prior to Jan 1, 1982 | BAUSCH | Discontinued |
| NORFLEX | 013055 | 001 | NDA | ORPHENADRINE CITRATE | INJECTABLE;INJECTION | 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 1960/10/02 | Approved Prior to Jan 1, 1982 | PAI HOLDINGS PHARM | Discontinued |