Visitor Monitoring Drug Details: RUFEN
 
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Drug Details

Drug Name: RUFEN
FDA Application No: (NDA) 018197
Active Ingredient(s): IBUPROFEN
Company: BASF
Original Approval or Tentative Approval Date: May 21, 1981
 
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
IBU IBUPROFEN400MGTABLET; ORAL Discontinued No None
RUFEN IBUPROFEN600MGTABLET; ORAL Discontinued No None


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