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: (ANDA) 070088
Active Ingredient(s): IBUPROFEN
Company: BASF
 
Label History
 
Labels are not available on this site for IBU, (ANDA) 070088
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/7/1988 008Labeling  
2/8/1988 007Labeling  
3/24/1987 006Chemistry  
3/24/1987 004Chemistry  
1/22/1986 003Chemistry  
4/9/1985 002Chemistry  
4/9/1985 001Chemistry  
2/8/1985 000Approval  
 
Therapeutic Equivalents
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