美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=OPANA
符合检索条件的记录共18
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1药品名称OPANA
申请号011707产品号001
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格1.5MG/ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ENDO PHARMACEUTICALS INC
2药品名称OPANA
申请号011707产品号002
活性成分OXYMORPHONE HYDROCHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格1MG/ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ENDO PHARMACEUTICALS INC
3药品名称OPANA ER
申请号021610产品号001
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期2006/06/22申请机构ENDO PHARMACEUTICALS INC
4药品名称OPANA ER
申请号021610产品号002
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期2006/06/22申请机构ENDO PHARMACEUTICALS INC
5药品名称OPANA ER
申请号021610产品号003
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格20MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期2006/06/22申请机构ENDO PHARMACEUTICALS INC
6药品名称OPANA ER
申请号021610产品号004
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格40MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期2006/06/22申请机构ENDO PHARMACEUTICALS INC
7药品名称OPANA ER
申请号021610产品号005
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期2008/02/29申请机构ENDO PHARMACEUTICALS INC
8药品名称OPANA ER
申请号021610产品号006
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期2008/02/29申请机构ENDO PHARMACEUTICALS INC
9药品名称OPANA ER
申请号021610产品号007
活性成分OXYMORPHONE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格30MG
治疗等效代码参比药物
批准日期2008/02/29申请机构ENDO PHARMACEUTICALS INC
10药品名称OPANA
申请号021611产品号001
活性成分OXYMORPHONE HYDROCHLORIDE市场状态处方药
剂型或给药途径TABLET;ORAL规格5MG
治疗等效代码AB参比药物
批准日期2006/06/22申请机构ENDO PHARMACEUTICALS INC