Visitor Monitoring Drug History: IBU
 
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: IBU
FDA Application No: (NDA) 018197
Active Ingredient(s): IBUPROFEN
Company: BASF
 
Label History
 
Labels are not available on this site for IBU, (NDA) 018197
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/6/1995 030Labeling  
1/5/1995 029Labeling  
10/9/1991 027Labeling  
10/25/1989 026Labeling  
1/19/1989 024Labeling  
10/28/1988 023Labeling  
1/17/1989 022Labeling  
7/1/1986 020Chemistry  
1/17/1986 019Chemistry  
1/17/1986 017Chemistry  
1/17/1986 016Chemistry  
1/17/1986 015Chemistry  
5/1/1985 012Chemistry  
5/21/1981 000Approval  
 
Therapeutic Equivalents
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