Visitor Monitoring Drug Details: ORUDIS
 
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Drug Details

Drug Name: ORUDIS
FDA Application No: (NDA) 018754
Active Ingredient(s): KETOPROFEN
Company: WYETH AYERST
Original Approval or Tentative Approval Date: January 9, 1986
Chemical Type: 1 New molecular entity (NME)
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
ORUDIS KETOPROFEN25MGCAPSULE; ORAL Discontinued No None
ORUDIS KETOPROFEN50MGCAPSULE; ORAL Discontinued No None
ORUDIS KETOPROFEN75MGCAPSULE; ORAL Discontinued No None


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