Visitor Monitoring Drug Details: ISUPREL
 
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Drug Details

Drug Name: ISUPREL
FDA Application No: (NDA) 006328
Active Ingredient(s): ISOPROTERENOL HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ISUPREL ISOPROTERENOL HYDROCHLORIDE10MGTABLET; RECTAL, SUBLINGUAL Discontinued No None
ISUPREL ISOPROTERENOL HYDROCHLORIDE15MGTABLET; RECTAL, SUBLINGUAL Discontinued No None


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