Visitor Monitoring Drug History: HIPREX
 
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: HIPREX
FDA Application No: (NDA) 017681
Active Ingredient(s): METHENAMINE HIPPURATE
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on November 30, 2005 for HIPREX, (NDA) 017681


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/21/2005 014Labeling Revision Letter
Label 
6/10/2004 013Labeling Revision Letter
Label 
8/9/1988 011Manufacturing Change or Addition  
4/28/1988 010Package Change  
1/3/1989 009Manufacturing Change or Addition  
5/3/1984 008Manufacturing Change or Addition  
4/25/1984 007Package Change  
5/26/1982 006Control Supplement  
3/19/1981 005Distributor  
11/25/1980 004Labeling Revision  
11/25/1980 003Labeling Revision  
2/27/1978 002Manufacturing Change or Addition  
2/24/1978 001Control Supplement  
9/9/1976 000Approval  
 
Therapeutic Equivalents
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