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) 070818
Active Ingredient(s): IBUPROFEN
Company: OHM LABS
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 070818
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/5/1994 013Chemistry  
8/22/1991 012Labeling in Effect  
9/21/1992 011Chemistry  
11/21/1991 010Chemistry  
11/21/1991 009Chemistry  
6/1/1989 008Labeling  
8/7/1990 007Chemistry  
3/16/1989 006Labeling  
1/10/1989 005Chemistry  
6/7/1988 004Chemistry  
5/11/1988 003Chemistry  
6/6/1988 002Chemistry  
2/11/1988 001Chemistry  
12/26/1985 000Approval  
 
Therapeutic Equivalents
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