Visitor Monitoring Drug Details: OMNIPAQUE 350
 
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Drug Details

Drug Name: OMNIPAQUE 350
FDA Application No: (NDA) 020608
Active Ingredient(s): IOHEXOL
Company: GE HEALTHCARE
Original Approval or Tentative Approval Date: October 24, 1995
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
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 240 IOHEXOL51.8%SOLUTION; INJECTION, ORAL, RECTAL Prescription No None
OMNIPAQUE 300 IOHEXOL64.7%SOLUTION; INJECTION, ORAL, RECTAL Prescription No None
OMNIPAQUE 350 IOHEXOL75.5%SOLUTION; INJECTION, ORAL Prescription No None


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