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) 073141
Active Ingredient(s): IBUPROFEN
Company: TEVA
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 073141
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/2/1999 009Facility Addition  
12/2/1999 008Facility Addition  
2/12/1999 003Chemistry  
2/12/1999 002Chemistry  
8/28/1998 001Chemistry  
5/29/1992 000Approval  
 
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