Visitor Monitoring Drug History: VANCENASE AQ
 
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: VANCENASE AQ
FDA Application No: (NDA) 020469
Active Ingredient(s): BECLOMETHASONE DIPROPIONATE MONOHYDRATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for VANCENASE AQ, (NDA) 020469
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/30/2000 008Control Supplement  
6/11/2002 007Control Supplement  
7/28/1998 006Package Change  
2/13/1997 003Labeling Revision  
2/13/1997 002Labeling Revision  
3/14/1997 001Manufacturing Change or Addition  
6/26/1996 000Approval  
 
There are no Therapeutic Equivalents
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