Visitor Monitoring Drug History: FORTAZ
 
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: FORTAZ
FDA Application No: (NDA) 050578
Active Ingredient(s): CEFTAZIDIME
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on July 10, 2007 for FORTAZ, (NDA) 050578


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
7/9/2007 053Labeling Revision Letter
Label 
3/14/2007 051Labeling Revision Label 
5/19/2004 046Labeling Revision Letter
Label 
10/23/2002 044Control Supplement  
2/22/2002 043Control Supplement  
3/22/2002 042Labeling Revision Letter 
3/29/2002 040Labeling Revision Letter
Label 
11/25/1997 039Control Supplement  
4/3/1997 038Manufacturing Change or Addition  
12/24/1996 037Labeling Revision  
10/4/1996 036Control Supplement  
11/3/1995 035Manufacturing Change or Addition  
6/20/1996 034Labeling Revision  
6/20/1996 033Labeling Revision  
1/26/1998 032Labeling Revision  
8/20/1996 031Labeling Revision  
9/11/1996 030Labeling Revision  
2/18/1993 029Manufacturing Change or Addition  
12/31/1992 028Labeling Revision  
10/20/1994 027Labeling Revision  
8/9/1991 026Manufacturing Change or Addition  
2/13/1992 024Package Change  
9/7/1994 022Labeling Revision  
2/13/1992 021Control Supplement  
3/22/1990 020Manufacturing Change or Addition  
4/10/1990 018Chemistry Generic  
4/29/1993 017Labeling Revision  
4/29/1993 015Labeling Revision  
7/19/1985 000Approval  
 
Therapeutic Equivalents
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