| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| SODIUM BUTABARBITAL | 085881 | 001 | ANDA | BUTABARBITAL SODIUM | TABLET;ORAL | 100MG | No | No | 1978/07/20 | Approved Prior to Jan 1, 1982 | LANNETT | Discontinued |
| SODIUM BUTABARBITAL | 085849 | 001 | ANDA | BUTABARBITAL SODIUM | TABLET;ORAL | 15MG | No | No | 1978/08/21 | Approved Prior to Jan 1, 1982 | LANNETT | Discontinued |
| BUTABARBITAL SODIUM | 085383 | 001 | ANDA | BUTABARBITAL SODIUM | ELIXIR;ORAL | 30MG/5ML | No | No | 1979/02/26 | Approved Prior to Jan 1, 1982 | WOCKHARDT | Discontinued |
| BUTABARBITAL SODIUM | 085934 | 001 | ANDA | BUTABARBITAL SODIUM | TABLET;ORAL | 30MG | No | No | 1994/09/16 | Approved Prior to Jan 1, 1982 | SANDOZ | Discontinued |
| BUTABARBITAL SODIUM | 085938 | 001 | ANDA | BUTABARBITAL SODIUM | TABLET;ORAL | 15MG | Yes | No | 1994/09/16 | Approved Prior to Jan 1, 1982 | SANDOZ | Discontinued |