Visitor Monitoring Drug Details: NUPRIN
 
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Drug Details

Drug Name: NUPRIN
FDA Application No: (NDA) 019012
Active Ingredient(s): IBUPROFEN
Company: MCNEIL
Original Approval or Tentative Approval Date: May 18, 1984
Chemical Type: 5 New manufacturer
Review Classification: S Standard 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
MOTRIN IB IBUPROFEN200MGTABLET; ORAL OTC Yes None
MOTRIN MIGRAINE PAIN IBUPROFEN200MGTABLET; ORAL OTC Yes None
NUPRIN IBUPROFEN200MGTABLET; ORAL Discontinued No None
NUPRIN IBUPROFEN200MGTABLET; ORAL Discontinued No None


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