Visitor Monitoring Drug History: TEMOVATE E
 
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: TEMOVATE E
FDA Application No: (NDA) 020340
Active Ingredient(s): CLOBETASOL PROPIONATE
Company: ALTANA
 
Label History
 
View the label approved on April 7, 2003 for TEMOVATE E, (NDA) 020340


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
4/2/2003 006Labeling Revision Letter
Label 
8/8/1997 004Manufacturing Change or Addition  
11/15/1996 003Manufacturing Change or Addition Review 
7/24/1995 002Labeling Revision  
5/3/1996 001New Dosage Regimen  
6/17/1994 000Approval  
 
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