共 1 页 当前第 1 页 返回检索页| 1 | 药品名称 | ATARAX |
| 申请号 | 010392 | 产品号 | 001 |
| 活性成分 | HYDROXYZINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET;ORAL | 规格 | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | PFIZER INC
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| 2 | 药品名称 | ATARAX |
| 申请号 | 010392 | 产品号 | 004 |
| 活性成分 | HYDROXYZINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET;ORAL | 规格 | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | PFIZER INC
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| 3 | 药品名称 | ATARAX |
| 申请号 | 010392 | 产品号 | 005 |
| 活性成分 | HYDROXYZINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET;ORAL | 规格 | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | PFIZER INC
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| 4 | 药品名称 | ATARAX |
| 申请号 | 010392 | 产品号 | 006 |
| 活性成分 | HYDROXYZINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET;ORAL | 规格 | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | PFIZER INC
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| 5 | 药品名称 | ATARAX |
| 申请号 | 010485 | 产品号 | 001 |
| 活性成分 | HYDROXYZINE HYDROCHLORIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | SYRUP;ORAL | 规格 | 10MG/5ML |
| 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 | ROERIG DIV PFIZER INC
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