Visitor Monitoring Drug History: ULTRAVATE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: ULTRAVATE
FDA Application No: (NDA) 019967
Active Ingredient(s): HALOBETASOL PROPIONATE
Company: RANBAXY
 
Label History
 
View the label approved on September 17, 2004 for ULTRAVATE, (NDA) 019967


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 010Labeling Revision Letter
Label 
10/4/1996 008Control Supplement  
10/27/1993 007Control Supplement  
2/10/1993 006Control Supplement  
7/14/1992 005Control Supplement  
4/2/2003 004Labeling Revision Letter
Label
Review 
12/30/1991 003Control Supplement  
8/25/1993 002Control Supplement  
12/31/1991 001New Dosage Regimen  
12/27/1990 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test