Visitor Monitoring Drug History: BECONASE AQ
 
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: BECONASE AQ
FDA Application No: (NDA) 019389
Active Ingredient(s): BECLOMETHASONE DIPROPIONATE MONOHYDRATE
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on November 1, 2005 for BECONASE AQ, (NDA) 019389


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
10/27/2005 027Labeling Revision Letter
Label 
3/4/2002 026Control Supplement  
12/16/2002 025Labeling Revision Letter 
7/9/2001 024Control Supplement  
8/31/2001 023Labeling Revision Label 
12/19/2002 021Labeling Revision Letter 
2/24/1999 020Manufacturing Change or Addition  
3/27/1998 019Manufacturing Change or Addition  
5/30/1997 017Labeling Revision  
11/26/1996 016Labeling Revision  
11/19/1993 012Labeling Revision  
8/10/1992 011Manufacturing Change or Addition  
10/6/1992 009Control Supplement  
5/15/1990 007Manufacturing Change or Addition  
9/7/1989 006Package Change  
3/9/1989 005Manufacturing Change or Addition  
12/19/1988 004Labeling Revision  
7/8/1988 003Manufacturing Change or Addition  
8/25/1989 002Control Supplement  
8/19/1988 001Expiration Date Change  
7/27/1987 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test