Visitor Monitoring Drug History: ZOVIRAX
 
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: ZOVIRAX
FDA Application No: (NDA) 018603
Active Ingredient(s): ACYCLOVIR SODIUM
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on May 27, 2004 for ZOVIRAX, (NDA) 018603


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
5/19/2004 027Labeling Revision Letter
Label 
1/29/2002 025Labeling Revision Letter 
1/29/2002 024Labeling Revision Letter 
1/29/2002 023Labeling Revision Letter 
7/12/2000 022Manufacturing Change or Addition  
7/15/1999 021Control Supplement  
5/19/1999 020Labeling Revision  
6/2/1998 019New or Modified Indication Letter
Label 
10/29/1996 018Control Supplement  
6/7/1995 017Manufacturing Change or Addition  
4/14/1994 015Labeling Revision  
11/9/1993 014Control Supplement  
4/22/1993 013Labeling Revision  
7/17/1992 012Control Supplement  
6/29/1989 011Package Change  
4/22/1993 010Labeling Revision  
2/9/1990 009New or Modified Indication  
7/9/1984 008Labeling Revision  
5/31/1984 007Manufacturing Change or Addition  
8/14/1984 006Expiration Date Change  
5/8/1984 005Manufacturing Change or Addition  
8/30/1983 004Manufacturing Change or Addition  
2/9/1990 003New or Modified Indication  
1/5/1983 002Expiration Date Change  
12/14/1982 001Control Supplement  
10/22/1982 000Approval  
 
Therapeutic Equivalents
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