Visitor Monitoring Drug Details: RELAFEN
 
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Drug Details

Drug Name: RELAFEN
FDA Application No: (NDA) 019583
Active Ingredient(s): NABUMETONE
Company: SMITHKLINE BEECHAM
Original Approval or Tentative Approval Date: December 24, 1991
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
 
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
RELAFEN NABUMETONE500MGTABLET; ORAL Discontinued No None
RELAFEN NABUMETONE750MGTABLET; ORAL Discontinued No None


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