| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72189-517-06 | 72189-517 | HUMAN PRESCRIPTION DRUG | Eletriptan HBR | Eletriptan HBR | TABLET, FILM COATED | ORAL | 20231011 | N/A | ANDA | ANDA210708 | Direct_Rx | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 6 TABLET, FILM COATED in 1 CARTON (72189-517-06) |
| 59651-105-93 | 59651-105 | HUMAN PRESCRIPTION DRUG | Eletriptan Hydrobromide | Eletriptan Hydrobromide | TABLET, FILM COATED | ORAL | 20190115 | N/A | ANDA | ANDA210708 | Aurobindo Pharma Limited | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 2 BLISTER PACK in 1 CARTON (59651-105-93) / 6 TABLET, FILM COATED in 1 BLISTER PACK |
| 59651-105-69 | 59651-105 | HUMAN PRESCRIPTION DRUG | Eletriptan Hydrobromide | Eletriptan Hydrobromide | TABLET, FILM COATED | ORAL | 20190115 | N/A | ANDA | ANDA210708 | Aurobindo Pharma Limited | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 1 BLISTER PACK in 1 CARTON (59651-105-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59651-105-06) |
| 59651-104-69 | 59651-104 | HUMAN PRESCRIPTION DRUG | Eletriptan Hydrobromide | Eletriptan Hydrobromide | TABLET, FILM COATED | ORAL | 20190115 | N/A | ANDA | ANDA210708 | Aurobindo Pharma Limited | ELETRIPTAN HYDROBROMIDE | 20 mg/1 | 1 BLISTER PACK in 1 CARTON (59651-104-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59651-104-06) |