Visitor Monitoring Drug Details: HEXABRIX
 
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Drug Details

Drug Name: HEXABRIX
FDA Application No: (NDA) 018905
Active Ingredient(s): IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM
Company: MALLINCKRODT
Original Approval or Tentative Approval Date: July 26, 1985
Chemical Type: 14 New molecular entity and new combination
Review Classification: S Standard review drug
 
 
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
HEXABRIX IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM39.3%; 19.6%INJECTABLE; INJECTION Prescription Yes None


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