Visitor Monitoring Drug History: MOTRIN
 
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Label and Approval History

Drug Name: MOTRIN
FDA Application No: (NDA) 020476
Active Ingredient(s): IBUPROFEN
Company: MCNEIL
 
Label History
 
Labels are not available on this site for MOTRIN, (NDA) 020476
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/14/2001 003Control Supplement  
2/4/2002 002Labeling Revision Letter
Review 
5/25/1995 000Approval  
 
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