Visitor Monitoring Drug History: IBUPROFEN
 
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: IBUPROFEN
FDA Application No: (ANDA) 070733
Active Ingredient(s): IBUPROFEN
Company: SANDOZ
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 070733
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/28/2000 013Package Change  
4/26/1989 011Chemistry  
6/29/1988 009Chemistry  
4/6/1988 007Labeling  
4/6/1988 006Chemistry  
11/3/1987 005Chemistry  
5/7/1987 004Chemistry  
5/7/1987 003Chemistry  
5/7/1987 002Chemistry  
5/7/1987 001Chemistry  
9/19/1986 000Approval  
 
Therapeutic Equivalents
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