Visitor Monitoring Drug History: UNIRETIC
 
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: UNIRETIC
FDA Application No: (NDA) 020729
Active Ingredient(s): HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
Company: SCHWARZ PHARMA
 
Label History
 
Labels are not available on this site for UNIRETIC, (NDA) 020729
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/29/2003 012Labeling Revision Letter 
2/14/2002 010Formulation Revision Letter
Review 
9/24/2001 009Control Supplement  
12/22/2000 008Package Change  
1/12/2001 007Manufacturing Change or Addition  
5/10/2000 006Manufacturing Change or Addition  
4/5/2000 005Labeling Revision  
10/29/1999 004Manufacturing Change or Addition  
4/22/1999 003Package Change  
1/21/1998 002Labeling Revision  
11/18/1997 001Manufacturing Change or Addition  
6/27/1997 000Approval  
 
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