产品NDC51662-1320
产品类型HUMAN PRESCRIPTION DRUG
商品名EPINEPHRINE
商品名后缀
通用名EPINEPHRINE
剂型INJECTION, SOLUTION
给药途径INTRAMUSCULAR
上市日期20180921
中止上市日期
市场分类NDA
申请号NDA201739
标签持有者HF Acquisition Co LLC, DBA HealthFirst
活性成分EPINEPHRINE
规格.3
规格单位mg/.3mL
药学分类Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
DEA N 20201231
药品包装规格及说明书信息
产品NDC NDC包装代码 包装描述 药品说明书
51662-132051662-1320-1.3 mL in 1 DOSE PACK (51662-1320-1) 20180921 N N药品说明书及标签信息
51662-132051662-1320-22 DOSE PACK in 1 CARTON (51662-1320-2) > .3 mL in 1 DOSE PACK 20190824 N N药品说明书及标签信息