美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=KYTRIL
符合检索条件的记录共7
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1药品名称KYTRIL
申请号020239产品号001
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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1993/12/29申请机构HOFFMANN LA ROCHE INC
2药品名称KYTRIL
申请号020239产品号002
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 4MG BASE/4ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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1994/03/11申请机构HOFFMANN LA ROCHE INC
3药品名称KYTRIL
申请号020239产品号003
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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2004/09/17申请机构HOFFMANN LA ROCHE INC
4药品名称KYTRIL
申请号020239产品号004
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 1MG BASE/ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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1994/03/11申请机构HOFFMANN LA ROCHE INC
5药品名称KYTRIL
申请号020305产品号001
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格EQ 1MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or efficacy reasons**
治疗等效代码参比药物
批准日期1995/03/16申请机构HOFFMANN LA ROCHE INC
6药品名称KYTRIL
申请号020305产品号002
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格EQ 2MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or efficacy reasons**
治疗等效代码参比药物
批准日期1998/06/15申请机构HOFFMANN LA ROCHE INC
7药品名称KYTRIL
申请号021238产品号001
活性成分GRANISETRON HYDROCHLORIDE市场状态停止上市
剂型或给药途径SOLUTION;ORAL规格EQ 2MG BASE/10ML
治疗等效代码参比药物
批准日期2001/06/27申请机构HOFFMANN LA ROCHE INC