Visitor Monitoring Drug History: CEPTAZ
 
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: CEPTAZ
FDA Application No: (NDA) 050646
Active Ingredient(s): CEFTAZIDIME (ARGININE FORMULATION)
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on March 29, 2002 for CEPTAZ, (NDA) 050646


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
2/22/2002 017Control Supplement  
2/23/2000 015Manufacturing Change or Addition  
3/29/2002 014Labeling Revision Letter
Label 
11/25/1997 013Control Supplement  
4/3/1997 012Manufacturing Change or Addition  
12/24/1996 011Labeling Revision  
6/20/1996 010Labeling Revision  
6/20/1996 009Labeling Revision  
1/26/1998 008Labeling Revision  
8/20/1996 007Labeling Revision  
9/11/1996 006Labeling Revision  
10/20/1994 005Labeling Revision  
9/7/1994 004Labeling Revision  
8/9/1991 003Manufacturing Change or Addition  
9/10/1992 002Control Supplement  
9/9/1992 001Package Change  
9/27/1990 000Approval  
 
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