| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0093-8311-18 | 0093-8311 | HUMAN PRESCRIPTION DRUG | Eletriptan Hydrobromide | Eletriptan Hydrobromide | TABLET, FILM COATED | ORAL | 20170721 | N/A | ANDA | ANDA202040 | Teva Pharmaceuticals USA, Inc. | ELETRIPTAN HYDROBROMIDE | 40 mg/1 | 6 BLISTER PACK in 1 CARTON (0093-8311-18) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-8311-19) |
| 0093-8310-18 | 0093-8310 | HUMAN PRESCRIPTION DRUG | Eletriptan Hydrobromide | Eletriptan Hydrobromide | TABLET, FILM COATED | ORAL | 20170721 | N/A | ANDA | ANDA202040 | Teva Pharmaceuticals USA, Inc. | ELETRIPTAN HYDROBROMIDE | 20 mg/1 | 6 BLISTER PACK in 1 CARTON (0093-8310-18) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-8310-19) |