Visitor Monitoring Drug Details: OMNIPAQUE 210
 
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Drug Details

Drug Name: OMNIPAQUE 210
FDA Application No: (NDA) 018956
Active Ingredient(s): IOHEXOL
Company: GE HEALTHCARE
Original Approval or Tentative Approval Date: December 26, 1985
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
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
OMNIPAQUE 140 IOHEXOL30.2%INJECTABLE; INJECTION Prescription Yes None
OMNIPAQUE 180 IOHEXOL38.8%SOLUTION; INJECTION, ORAL, RECTAL Prescription Yes None
OMNIPAQUE 210 IOHEXOL45.3%INJECTABLE; INJECTION Discontinued No None
OMNIPAQUE 240 IOHEXOL51.8%SOLUTION; INJECTION, ORAL, RECTAL Prescription Yes None
OMNIPAQUE 300 IOHEXOL64.7%SOLUTION; INJECTION, ORAL, RECTAL Prescription Yes None
OMNIPAQUE 350 IOHEXOL75.5%SOLUTION; INJECTION, ORAL Prescription Yes None
OMNIPAQUE 70 IOHEXOL15.1%SOLUTION; URETHRAL Discontinued No None


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