Visitor Monitoring Drug History: ESTRADERM
 
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: ESTRADERM
FDA Application No: (NDA) 019081
Active Ingredient(s): ESTRADIOL
Company: NOVARTIS
 
Label History
 
View the label approved on December 30, 2004 for ESTRADERM, (NDA) 019081


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
12/17/2004 040Labeling Revision Letter
Label 
5/28/2004 039Labeling Revision Letter
Label 
5/28/2004 036Labeling Revision Letter
Label 
3/14/2002 035Manufacturing Change or Addition  
8/20/2001 034Manufacturing Change or Addition  
12/10/1997 031Labeling Revision  
6/27/1996 029Control Supplement  
6/27/1996 028Control Supplement  
12/7/1995 027Labeling Revision  
11/28/1995 026Labeling Revision  
1/20/1995 025Manufacturing Change or Addition  
2/10/1995 024Formulation Revision  
5/18/1994 023Formulation Revision  
4/5/1993 022Labeling Revision  
8/9/1993 021Control Supplement  
9/22/1995 020Labeling Revision  
1/22/1992 019Control Supplement  
10/24/1991 018New or Modified Indication  
6/12/1990 017Manufacturing Change or Addition  
6/19/1990 015Labeling Revision  
6/18/1990 014Control Supplement  
1/19/1990 013Formulation Revision  
2/3/1989 011Manufacturing Change or Addition  
7/1/1988 010Control Supplement  
5/25/1988 009Package Change  
4/28/1988 008Labeling Revision  
7/7/1987 007Labeling Revision  
1/7/1988 006Manufacturing Change or Addition  
1/7/1988 005Manufacturing Change or Addition  
1/7/1988 004Manufacturing Change or Addition  
1/7/1988 003Manufacturing Change or Addition  
2/26/1987 002Labeling Revision  
12/3/1986 001Control Supplement  
9/10/1986 000Approval  
 
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