Visitor Monitoring Drug History: REPREXAIN
 
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: REPREXAIN
FDA Application No: (ANDA) 076642
Active Ingredient(s): HYDROCODONE BITARTRATE; IBUPROFEN
Company: INTERPHARM
 
Label History
 
Labels are not available on this site for REPREXAIN, (ANDA) 076642
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/19/2007 008Labeling Letter 
10/19/2007 007Chemistry New Strength Letter 
10/19/2007 006Labeling Letter 
10/19/2007 005Chemistry New Strength Letter 
10/12/2004 003Supplement  
3/18/2004 000Tentative Approval  
3/18/2004 000Approval  
 
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