Visitor Monitoring Drug History: ULTRAVATE
 
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Label and Approval History

Drug Name: ULTRAVATE
FDA Application No: (NDA) 019968
Active Ingredient(s): HALOBETASOL PROPIONATE
Company: RANBAXY
 
Label History
 
View the label approved on September 17, 2004 for ULTRAVATE, (NDA) 019968


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
9/17/2004 007Labeling Revision Letter
Label 
7/12/1995 005Control Supplement  
10/27/1993 004Control Supplement  
11/4/1993 003Control Supplement  
2/10/1993 002Control Supplement  
12/31/1991 001New Dosage Regimen  
12/17/1990 000Approval  
 
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