Visitor Monitoring Drug Details: MOTRIN
 
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Drug Details

Drug Name: MOTRIN
FDA Application No: (NDA) 017463
Active Ingredient(s): IBUPROFEN
Company: MCNEIL PED
Original Approval or Tentative Approval Date: September 19, 1974
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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 IBUPROFEN400MGTABLET; ORAL Prescription No AB
MOTRIN IBUPROFEN300MGTABLET; ORAL Prescription No AB
MOTRIN IBUPROFEN600MGTABLET; ORAL Prescription No AB
MOTRIN IBUPROFEN800MGTABLET; ORAL Prescription Yes AB


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