Visitor Monitoring Drug History: WESTCORT
 
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: WESTCORT
FDA Application No: (NDA) 017950
Active Ingredient(s): HYDROCORTISONE VALERATE
Company: RANBAXY
 
Label History
 
View the label approved on March 25, 2003 for WESTCORT, (NDA) 017950


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
3/24/2003 021Labeling Revision Letter
Label 
11/29/1991 019Formulation Revision  
10/4/1988 018Control Supplement  
8/27/1986 017Control Supplement  
8/13/1985 016Package Change  
1/3/1985 015Control Supplement  
2/15/1984 014Package Change  
10/5/1983 013Control Supplement  
5/6/1983 012Control Supplement  
9/8/1982 011Package Change  
8/27/1981 010Manufacturing Change or Addition  
1/28/1983 009Practioner Draft Labeling  
9/8/1982 008Expiration Date Change  
5/14/1980 006Control Supplement  
3/6/1980 005Control Supplement  
1/10/1980 004Expiration Date Change  
4/10/1979 003Control Supplement  
12/11/1978 002Control Supplement  
3/17/1978 000Approval  
 
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