Visitor Monitoring Drug Details: DIATRIZOATE MEGLUMINE
 
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Drug Details

Drug Name: DIATRIZOATE MEGLUMINE
FDA Application No: (NDA) 010040
Active Ingredient(s): DIATRIZOATE MEGLUMINE
Company: BRACCO
Original Approval or Tentative Approval Date: August 2, 1955
Chemical Type: 24 New ative ingredient and new combination
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
CYSTOGRAFIN DIATRIZOATE MEGLUMINE30%SOLUTION; URETHRAL Prescription No AT
CYSTOGRAFIN DILUTE DIATRIZOATE MEGLUMINE18%SOLUTION; URETHRAL Prescription No None
DIATRIZOATE MEGLUMINE DIATRIZOATE MEGLUMINE76%INJECTABLE; INJECTION Discontinued No None
RENO-30 DIATRIZOATE MEGLUMINE30%SOLUTION; URETERAL Prescription No None
RENO-60 DIATRIZOATE MEGLUMINE60%INJECTABLE; INJECTION Prescription Yes AP
RENO-DIP DIATRIZOATE MEGLUMINE30%INJECTABLE; INJECTION Prescription Yes None
RENOGRAFIN-60 DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM52%; 8%INJECTABLE; INJECTION Prescription Yes None
RENOGRAFIN-76 DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM66%; 10%INJECTABLE; INJECTION Prescription Yes AP
RENOVIST DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM34.3%; 35%INJECTABLE; INJECTION Discontinued No None
RENOVIST II DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM28.5%; 29.1%INJECTABLE; INJECTION Discontinued No None


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