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) 071333
Active Ingredient(s): IBUPROFEN
Company: INTERPHARM
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 071333
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/22/2002 026Labeling  
9/25/2001 025Manufacturing Revision  
3/13/2001 024Labeling  
12/4/2000 023Facility Addition  
4/12/2000 022Control Supplement  
4/12/2000 021Manufacturing Revision  
9/13/1999 020Labeling  
4/12/2000 019Facility Addition  
9/24/1999 017Chemistry  
2/11/1999 016Chemistry  
7/25/2000 015Labeling  
7/25/2000 014Chemistry  
7/25/2000 013Chemistry  
7/25/2000 012Chemistry  
7/24/1997 010Chemistry  
11/22/1994 009Labeling  
1/20/1998 008Chemistry  
7/26/1988 007Chemistry  
4/5/1988 006Chemistry  
4/5/1988 005Chemistry  
4/5/1988 004Chemistry  
10/8/1987 003Chemistry  
2/17/1988 002Chemistry  
6/24/1987 001Chemistry  
2/17/1987 000Approval  
 
Therapeutic Equivalents
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