Visitor Monitoring Drug Details: AZULFIDINE EN-TABS
 
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Drug Details

Drug Name: AZULFIDINE EN-TABS
FDA Application No: (NDA) 007073
Active Ingredient(s): SULFASALAZINE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: June 20, 1950
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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
AZULFIDINE SULFASALAZINE500MGTABLET; ORAL Prescription Yes AB
AZULFIDINE EN-TABS SULFASALAZINE500MGTABLET, DELAYED RELEASE; ORAL Prescription Yes AB


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On Wednesday, August 6, 2014 yvonne wrote:
 
can azulfidine or sulfasaazine affect a drug test
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