Visitor Monitoring Drug History: VEPESID
 
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: VEPESID
FDA Application No: (NDA) 018768
Active Ingredient(s): ETOPOSIDE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
View the label approved on April 7, 2003 for VEPESID, (NDA) 018768


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
10/25/2000 046Manufacturing Change or Addition  
11/5/2002 045Labeling Revision Letter
Review 
2/2/2000 044Formulation Revision  
4/2/1999 041Labeling Revision Review 
12/15/1998 040Control Supplement  
12/11/1995 037Control Supplement  
8/8/1995 036Control Supplement  
6/27/1995 035Control Supplement  
8/30/1993 032Manufacturing Change or Addition  
12/20/1993 031Manufacturing Change or Addition  
7/23/1993 030Labeling Revision  
8/24/1993 028Control Supplement  
5/17/1995 027Control Supplement  
11/1/1991 026Labeling Revision  
11/1/1991 025Labeling Revision  
9/4/1990 024Control Supplement  
4/4/1990 023Manufacturing Change or Addition  
4/10/1989 022Control Supplement  
2/11/1988 018Control Supplement  
1/25/1988 017Labeling Revision  
5/20/1987 016Labeling Revision  
4/28/1988 015Manufacturing Change or Addition  
3/19/1987 014Manufacturing Change or Addition  
12/22/1986 013Labeling Revision  
10/29/1986 012Manufacturing Change or Addition  
6/30/1986 011Manufacturing Change or Addition  
8/26/1986 010Labeling Revision  
11/6/1986 009Manufacturing Change or Addition  
9/4/1986 007New or Modified Indication Label 
3/12/1985 006Control Supplement  
3/6/1985 005Labeling Revision  
3/6/1985 004Labeling Revision  
3/6/1985 003Labeling Revision  
3/6/1985 002Labeling Revision  
8/21/1984 001Control Supplement  
11/10/1983 000Approval Label 
 
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