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) 070745
Active Ingredient(s): IBUPROFEN
Company: BASF
 
Label History
 
Labels are not available on this site for IBU, (ANDA) 070745
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/27/1995 015Labeling  
2/15/1995 014Labeling  
8/11/1995 013Chemistry  
9/30/1994 011Chemistry  
9/30/1994 010Chemistry  
10/17/1991 009Labeling  
8/6/1991 008Labeling  
10/27/1989 007Labeling  
6/8/1989 006Labeling  
1/10/1989 005Labeling  
1/27/1989 004Chemistry  
10/7/1988 003Labeling  
3/1/1988 002Labeling  
9/3/1986 001Labeling  
7/23/1986 000Approval  
 
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