Visitor Monitoring Drug Details: HYPAQUE
 
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Drug Details

Drug Name: HYPAQUE
FDA Application No: (NDA) 011386
Active Ingredient(s): DIATRIZOATE SODIUM
Company: GE HEALTHCARE
Original Approval or Tentative Approval Date: March 26, 1956
Chemical Type: 3 New dosage form
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
HYPAQUE DIATRIZOATE SODIUM100%FOR SOLUTION; ORAL, RECTAL Prescription No None
HYPAQUE DIATRIZOATE SODIUM40%SOLUTION; ORAL, RECTAL Discontinued No None


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