| 1 | 药品名称 | NORTREL 7/7/7 | ||
| 申请号 | 075478 | 产品号 | 001 | |
| 活性成分 | ETHINYL ESTRADIOL; NORETHINDRONE | 市场状态 | 处方药 | |
| 剂型或给药途径 | TABLET;ORAL-21 | 规格 | 0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG | |
| 治疗等效代码 | 参比药物 | 否 | ||
| 批准日期 | 2002/08/30 | 申请机构 | BARR LABORATORIES INC | |
| 2 | 药品名称 | NORTREL 7/7/7 | ||
| 申请号 | 075478 | 产品号 | 002 | |
| 活性成分 | ETHINYL ESTRADIOL; NORETHINDRONE | 市场状态 | 处方药 | |
| 剂型或给药途径 | TABLET;ORAL-28 | 规格 | 0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG | |
| 治疗等效代码 | AB | 参比药物 | 否 | |
| 批准日期 | 2002/08/30 | 申请机构 | BARR LABORATORIES INC | |
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