| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| SUBUTEX | 020732 | 002 | NDA | BUPRENORPHINE HYDROCHLORIDE | TABLET;SUBLINGUAL | EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 2002/10/08 | 2002/10/08 | INDIVIOR | Discontinued |
| SUBUTEX | 020732 | 003 | NDA | BUPRENORPHINE HYDROCHLORIDE | TABLET;SUBLINGUAL | EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 2002/10/08 | 2002/10/08 | INDIVIOR | Discontinued |