共 1 页 当前第 1 页 返回检索页| 1 | 药品名称 | DURANEST |
| 申请号 | 017751 | 产品号 | 003 |
| 活性成分 | ETIDOCAINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | ASTRAZENECA LP
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| 2 | 药品名称 | DURANEST |
| 申请号 | 017751 | 产品号 | 004 |
| 活性成分 | EPINEPHRINE; ETIDOCAINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 0.005MG/ML;0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | ASTRAZENECA LP
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| 3 | 药品名称 | DURANEST |
| 申请号 | 017751 | 产品号 | 005 |
| 活性成分 | ETIDOCAINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 1% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | ASTRAZENECA LP
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| 4 | 药品名称 | DURANEST |
| 申请号 | 017751 | 产品号 | 006 |
| 活性成分 | EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 0.005MG/ML;1% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | ASTRAZENECA LP
|
| 5 | 药品名称 | DURANEST |
| 申请号 | 017751 | 产品号 | 007 |
| 活性成分 | EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 0.005MG/ML;1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | ASTRAZENECA LP
|
| 6 | 药品名称 | DURANEST |
| 申请号 | 021384 | 产品号 | 001 |
| 活性成分 | EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 0.005MG/ML;1.5% |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | DENTSPLY PHARMACEUTICAL
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