Visitor Monitoring Drug History: DIPROSONE
 
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: DIPROSONE
FDA Application No: (NDA) 017536
Active Ingredient(s): BETAMETHASONE DIPROPIONATE
Company: SCHERING
 
Label History
 
View the label approved on October 3, 2001 for DIPROSONE, (NDA) 017536


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
1/10/2002 025Control Supplement  
10/3/2001 024Patient Population Altered Letter
Label
Review 
5/14/1999 023Control Supplement  
11/10/1998 022Package Change  
12/7/1998 021Control Supplement  
7/31/1998 020Control Supplement  
6/15/1998 019Control Supplement  
10/3/2001 018Labeling Revision Letter
Label
Review 
8/1/1990 017Control Supplement  
10/29/1987 016Manufacturing Change or Addition  
9/12/1986 015Manufacturing Change or Addition  
5/20/1986 014Control Supplement  
4/23/1986 013Manufacturing Change or Addition  
6/12/1984 012Manufacturing Change or Addition  
4/19/1982 010Manufacturing Change or Addition  
7/21/1982 009General Efficacy (MarkIV)  
9/2/1981 008Manufacturing Change or Addition  
10/13/1981 006Formulation Revision  
12/26/1979 005Distributor  
7/6/1979 004Control Supplement  
6/3/1980 003Control Supplement  
9/29/1978 002Labeling Revision  
3/17/1975 001Labeling Revision  
1/29/1975 000Approval  
 
Therapeutic Equivalents
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