Visitor Monitoring Drug History: DIPROLENE
 
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: DIPROLENE
FDA Application No: (NDA) 019408
Active Ingredient(s): BETAMETHASONE DIPROPIONATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for DIPROLENE, (NDA) 019408
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/14/1999 014Control Supplement  
11/10/1998 013Package Change  
6/15/1998 012Control Supplement  
7/31/1998 011Control Supplement  
6/15/1998 010Control Supplement  
11/30/1995 008Control Supplement  
12/8/1993 007Control Supplement  
11/22/1991 006Formulation Revision  
8/1/1990 005Control Supplement  
5/24/1989 004Labeling Revision  
2/24/1987 002Manufacturing Change or Addition  
5/13/1986 001Control Supplement  
1/31/1986 000Approval  
 
There are no Therapeutic Equivalents
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