Visitor Monitoring Drug History: LEVAQUIN
 
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: LEVAQUIN
FDA Application No: (NDA) 021721
Active Ingredient(s): LEVOFLOXACIN
Company: ORTHO MCNEIL PHARM
 
Label History
 
View the label approved on June 27, 2007 for LEVAQUIN, (NDA) 021721


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
6/19/2007 013Labeling Revision Letter
Label 
5/10/2007 012Labeling Revision Letter
Label 
9/11/2007 011Patient Population Altered Letter
Label 
5/31/2007 010Labeling Revision Letter
Label 
9/14/2007 009New Dosage Regimen Letter
Label 
6/23/2006 007Labeling Revision Letter
Label 
1/20/2006 006Labeling Revision Letter
Label 
11/24/2004 003New or Modified Indication Letter
Label 
8/4/2005 002New Dosage Regimen Letter
Label 
10/21/2004 000Approval Letter
Label
Review 
 
There are no Therapeutic Equivalents
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