Visitor Monitoring Drug History: MOTRIN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: MOTRIN
FDA Application No: (NDA) 020135
Active Ingredient(s): IBUPROFEN
Company: MCNEIL PED
 
Label History
 
Labels are not available on this site for MOTRIN, (NDA) 020135
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/5/2002 007Control Supplement  
5/14/2001 006Control Supplement  
2/4/2002 005Labeling Revision Letter
Review 
1/2/1996 002Control Supplement  
3/24/1995 001New or Modified Indication  
11/16/1994 000Approval  
 
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