| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| PHENYLBUTAZONE | 086151 | 001 | ANDA | PHENYLBUTAZONE | TABLET;ORAL | 100MG | No | No | 1979/10/29 | Approved Prior to Jan 1, 1982 | WATSON LABS | Discontinued |
| PHENYLBUTAZONE | 084339 | 001 | ANDA | PHENYLBUTAZONE | TABLET;ORAL | 100MG | No | No | 1980/01/10 | Approved Prior to Jan 1, 1982 | FOSUN PHARMA | Discontinued |
| PHENYLBUTAZONE | 087674 | 001 | ANDA | PHENYLBUTAZONE | TABLET;ORAL | 100MG | No | No | 1982/04/21 | 1982/04/21 | WATSON LABS | Discontinued |
| PHENYLBUTAZONE | 087774 | 001 | ANDA | PHENYLBUTAZONE | CAPSULE;ORAL | 100MG | No | No | 1982/06/16 | 1982/06/16 | CHARTWELL RX | Discontinued |
| PHENYLBUTAZONE | 087756 | 001 | ANDA | PHENYLBUTAZONE | CAPSULE;ORAL | 100MG | No | No | 1982/12/17 | 1982/12/17 | WATSON LABS | Discontinued |
| PHENYLBUTAZONE | 088218 | 001 | ANDA | PHENYLBUTAZONE | CAPSULE;ORAL | 100MG | No | No | 1983/06/24 | 1983/06/24 | IVAX PHARMS | Discontinued |
| PHENYLBUTAZONE | 088863 | 001 | ANDA | PHENYLBUTAZONE | TABLET;ORAL | 100MG | No | No | 1985/12/04 | 1985/12/04 | SUN PHARM INDUSTRIES | Discontinued |
| PHENYLBUTAZONE | 088994 | 001 | ANDA | PHENYLBUTAZONE | CAPSULE;ORAL | 100MG | No | No | 1985/12/04 | 1985/12/04 | SUN PHARM INDUSTRIES | Discontinued |