Visitor Monitoring Drug History: ZEBETA
 
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: ZEBETA
FDA Application No: (NDA) 019982
Active Ingredient(s): BISOPROLOL FUMARATE
Company: DURAMED PHARMS BARR
 
Label History
 
Labels are not available on this site for ZEBETA, (NDA) 019982
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/25/2007 014Labeling Revision Letter 
1/24/2003 010Labeling Revision Letter 
4/4/2000 007Labeling Revision  
2/19/1998 006Package Change Review 
6/23/1998 005Manufacturing Change or Addition Review 
1/14/1997 004Manufacturing Change or Addition Review 
5/30/1995 003Labeling Revision Review 
6/11/1993 001Expiration Date Change Review 
7/31/1992 000Approval Review 
 
Therapeutic Equivalents
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