Visitor Monitoring Drug History: ZIAC
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: ZIAC
FDA Application No: (NDA) 020186
Active Ingredient(s): BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Company: DURAMED PHARMS BARR
 
Label History
 
Labels are not available on this site for ZIAC, (NDA) 020186
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/25/2007 023Labeling Revision Letter 
1/24/2003 015Labeling Revision Letter 
4/4/2000 011Labeling Revision  
6/22/1999 010Control Supplement  
2/16/1999 009Manufacturing Change or Addition  
4/1/1998 008Labeling Revision  
1/15/1998 007Package Change  
10/9/1996 006Control Supplement  
4/24/1996 005Labeling Revision  
5/30/1995 004Labeling Revision Review 
4/15/1994 003Control Supplement  
11/24/1993 002Control Supplement  
9/7/1993 001Expiration Date Change  
3/26/1993 000Approval  
 
There are no Therapeutic Equivalents
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