Visitor Monitoring Drug Details: ULTRAVIST 300
 
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Drug Details

Drug Name: ULTRAVIST 300
FDA Application No: (NDA) 020220
Active Ingredient(s): IOPROMIDE
Company: BAYER HLTHC
Original Approval or Tentative Approval Date: May 10, 1995
Chemical Type: 1 New molecular entity (NME)
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
ULTRAVIST 150 IOPROMIDE31.2%INJECTABLE; INJECTION Prescription Yes None
ULTRAVIST 240 IOPROMIDE49.9%INJECTABLE; INJECTION Prescription Yes None
ULTRAVIST 300 IOPROMIDE62.3%INJECTABLE; INJECTION Prescription Yes None
ULTRAVIST 370 IOPROMIDE76.9%INJECTABLE; INJECTION Prescription Yes None


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