Visitor Monitoring Drug Details: ULTRAVIST 150
 
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Drug Details

Drug Name: ULTRAVIST 150
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
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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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