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) 075139
Active Ingredient(s): IBUPROFEN
Company: LNK
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 075139
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/4/2005 008Supplement Review 
7/19/2004 007Supplement Review 
2/4/2003 006Supplement Review 
8/5/2003 005Supplement Review 
8/15/2002 004Labeling Review 
2/11/2002 003Control Supplement Review 
2/11/2002 002Labeling Review 
8/15/2001 001Manufacturing Revision Review 
3/1/1999 000Approval Letter
Review 
 
Therapeutic Equivalents
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