Visitor Monitoring Drug History: TEMOVATE
 
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Label and Approval History

Drug Name: TEMOVATE
FDA Application No: (NDA) 020337
Active Ingredient(s): CLOBETASOL PROPIONATE
Company: ALTANA
 
Label History
 
View the label approved on April 7, 2003 for TEMOVATE, (NDA) 020337


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 005Labeling Revision Letter
Label 
6/5/1998 003Control Supplement  
8/8/1997 002Manufacturing Change or Addition  
11/15/1996 001Manufacturing Change or Addition Review 
4/29/1994 000Approval  
 
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