Visitor Monitoring Drug History: ELOCON
 
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: ELOCON
FDA Application No: (NDA) 019625
Active Ingredient(s): MOMETASONE FUROATE
Company: SCHERING
 
Label History
 
View the label approved on July 17, 2002 for ELOCON, (NDA) 019625


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
7/17/2002 013Patient Population Altered Letter
Label 
7/17/2002 012Labeling Revision Letter
Label 
4/13/2000 011Control Supplement  
11/10/1998 010Package Change  
12/28/1998 009Manufacturing Change or Addition  
6/5/1998 008Manufacturing Change or Addition  
5/21/1998 007Control Supplement  
3/7/1997 006Package Change  
4/16/1996 005Control Supplement  
9/25/1991 004Control Supplement  
10/3/1995 003Patient Population Altered  
10/29/1987 001Manufacturing Change or Addition  
5/6/1987 000Approval  
 
Therapeutic Equivalents
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