| NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0049-2330-45 | 0049-2330 | HUMAN PRESCRIPTION DRUG | Relpax | eletriptan hydrobromide | TABLET, FILM COATED | ORAL | 20021226 | N/A | NDA | NDA021016 | ROERIG | ELETRIPTAN HYDROBROMIDE | 20 mg/1 | 6 BLISTER PACK in 1 CARTON (0049-2330-45) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0049-2330-79) |
| 0049-2340-05 | 0049-2340 | HUMAN PRESCRIPTION DRUG | Relpax | eletriptan hydrobromide | TABLET, FILM COATED | ORAL | 20021226 | N/A | NDA | NDA021016 | ROERIG | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 12 BLISTER PACK in 1 CARTON (0049-2340-05) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0049-2340-79) |
| 0049-2340-45 | 0049-2340 | HUMAN PRESCRIPTION DRUG | Relpax | eletriptan hydrobromide | TABLET, FILM COATED | ORAL | 20021226 | 20250731 | NDA | NDA021016 | ROERIG | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 6 BLISTER PACK in 1 CARTON (0049-2340-45) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0049-2340-79) |
| 58151-368-56 | 58151-368 | HUMAN PRESCRIPTION DRUG | Relpax | eletriptan hydrobromide | TABLET | ORAL | 20240821 | N/A | NDA | NDA021016 | Viatris Specialty LLC | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 6 BLISTER PACK in 1 CARTON (58151-368-56) / 1 TABLET in 1 BLISTER PACK |