Visitor Monitoring Drug Details: KETOPROFEN
 
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Drug Details

Drug Name: KETOPROFEN
FDA Application No: (ANDA) 075679
Active Ingredient(s): KETOPROFEN
Company: MYLAN
Original Approval or Tentative Approval Date: February 20, 2002
 
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
KETOPROFEN KETOPROFEN200MGCAPSULE, EXTENDED RELEASE; ORAL Prescription Yes AB
KETOPROFEN KETOPROFEN150MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB
KETOPROFEN KETOPROFEN100MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB


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