Visitor Monitoring Drug History: TEQUIN
 
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: TEQUIN
FDA Application No: (NDA) 021061
Active Ingredient(s): GATIFLOXACIN
Company: BRISTOL MYERS SQUIBB
 
Label History
 
View the label approved on September 15, 2004 for TEQUIN, (NDA) 021061


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
3/29/2006 027Labeling Revision Letter 
12/9/2005 026Labeling Revision Letter 
9/14/2004 024Labeling Revision Letter
Label 
9/14/2004 023Labeling Revision Letter
Label 
6/30/2004 022New or Modified Indication Letter
Label 
1/6/2004 020Labeling Revision Letter
Label 
1/6/2004 019Labeling Revision Letter
Label 
12/12/2002 018Manufacturing Change or Addition  
10/23/2002 017Manufacturing Change or Addition  
10/17/2002 016Labeling Revision Letter
Label
Review 
12/19/2002 015Labeling Revision Letter
Label 
4/22/2002 014Manufacturing Change or Addition  
1/3/2002 013Manufacturing Change or Addition  
10/31/2001 012Labeling Revision Label 
12/19/2002 011Package Change Letter
Label 
10/17/2002 010Labeling Revision Letter
Label
Review 
10/31/2001 009Labeling Revision Label 
10/31/2001 008Labeling Revision Label 
10/12/2001 007New Dosage Regimen Letter
Label
Review 
8/20/2001 006Labeling Revision Label 
8/20/2001 005Labeling Revision Label 
12/13/2000 004Manufacturing Change or Addition  
6/20/2000 001Package Change  
12/17/1999 000Approval Letter
Label
Review
Other Important Information from FDA 
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test