Visitor Monitoring Drug History: FAMVIR
 
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: FAMVIR
FDA Application No: (NDA) 020363
Active Ingredient(s): FAMCICLOVIR
Company: NOVARTIS
 
Label History
 
View the label approved on August 4, 2006 for FAMVIR, (NDA) 020363


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
7/28/2006 028New or Modified Indication Letter
Label 
7/28/2006 027New Dosage Regimen Letter
Label 
2/22/2006 026Labeling Revision Letter
Label 
8/6/2002 020Manufacturing Change or Addition  
3/29/2001 019Labeling Revision Letter
Label
Review 
2/2/1999 017Control Supplement  
6/12/1998 016Labeling Revision Letter 
3/26/1998 015Control Supplement  
6/12/1998 014New or Modified Indication Letter 
7/15/1997 013Labeling Revision  
9/17/1997 012New or Modified Indication  
1/31/1997 011Manufacturing Change or Addition  
6/12/1998 010Labeling Revision Letter 
1/13/1997 009Labeling Revision  
4/26/1996 008Labeling Revision  
7/29/1996 007Labeling Revision  
9/8/1995 006Manufacturing Change or Addition  
7/29/1996 005Labeling Revision  
12/11/1995 004New or Modified Indication  
12/27/1994 001Manufacturing Change or Addition  
6/29/1994 000Approval  
 
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