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剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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| INJECTABLE;INJECTION | 规格 | 0.005MG/ML;0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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剂型或给药途径 | INJECTABLE;INJECTION | 规格 | 1% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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| INJECTABLE;INJECTION | 规格 | 0.005MG/ML;1% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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
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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| INJECTABLE;INJECTION | 规格 | 0.005MG/ML;1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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
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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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