美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=PRONESTYL
符合检索条件的记录共9
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1药品名称PRONESTYL
申请号007335产品号001
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径CAPSULE;ORAL规格250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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APOTHECON INC DIV BRISTOL MYERS SQUIBB
2药品名称PRONESTYL
申请号007335产品号002
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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APOTHECON INC DIV BRISTOL MYERS SQUIBB
3药品名称PRONESTYL
申请号007335产品号003
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径CAPSULE;ORAL规格500MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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APOTHECON INC DIV BRISTOL MYERS SQUIBB
4药品名称PRONESTYL
申请号007335产品号004
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径CAPSULE;ORAL规格375MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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APOTHECON INC DIV BRISTOL MYERS SQUIBB
5药品名称PRONESTYL
申请号007335产品号005
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格500MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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APOTHECON INC DIV BRISTOL MYERS SQUIBB
6药品名称PRONESTYL
申请号017371产品号001
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格250MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构APOTHECON INC DIV BRISTOL MYERS SQUIBB
7药品名称PRONESTYL
申请号017371产品号002
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格375MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构APOTHECON INC DIV BRISTOL MYERS SQUIBB
8药品名称PRONESTYL
申请号017371产品号003
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格500MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构APOTHECON INC DIV BRISTOL MYERS SQUIBB
9药品名称PRONESTYL-SR
申请号087361产品号001
活性成分PROCAINAMIDE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格500MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构APOTHECON INC DIV BRISTOL MYERS SQUIBB