美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DECADRON"
符合检索条件的记录共16
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11药品名称DECADRON
申请号012071产品号004
活性成分DEXAMETHASONE SODIUM PHOSPHATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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Approved Prior to Jan 1, 1982申请机构MERCK AND CO INC
12药品名称DECADRON
申请号012376产品号002
活性成分DEXAMETHASONE市场状态停止上市
剂型或给药途径ELIXIR;ORAL规格0.5MG/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MERCK AND CO INC
13药品名称DECADRON W/ XYLOCAINE
申请号013334产品号002
活性成分DEXAMETHASONE SODIUM PHOSPHATE; LIDOCAINE HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 4MG PHOSPHATE/ML;10MG/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MERCK AND CO INC
14药品名称DECADRON-LA
申请号016675产品号001
活性成分DEXAMETHASONE ACETATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 8MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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Approved Prior to Jan 1, 1982申请机构MERCK RESEARCH LABORATORIES DIV MERCK CO INC
15药品名称NEODECADRON
申请号050322产品号001
活性成分DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE市场状态停止上市
剂型或给药途径SOLUTION/DROPS;OPHTHALMIC规格EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/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MERCK AND CO INC
16药品名称NEODECADRON
申请号050324产品号001
活性成分DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE市场状态停止上市
剂型或给药途径OINTMENT;OPHTHALMIC规格EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MERCK AND CO INC