Visitor Monitoring Drug Details: IMURAN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: IMURAN
FDA Application No: (NDA) 017391
Active Ingredient(s): AZATHIOPRINE SODIUM
Company: PROMETHEUS LABS
Original Approval or Tentative Approval Date: July 19, 1974
Chemical Type: 3 New dosage form
Review Classification: P Priority 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
IMURAN AZATHIOPRINE SODIUMEQ 100MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None


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