Visitor Monitoring Drug History: DECADRON
 
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: DECADRON
FDA Application No: (NDA) 011984
Active Ingredient(s): DEXAMETHASONE SODIUM PHOSPHATE
Company: MERCK
 
Label History
 
Labels are not available on this site for DECADRON, (NDA) 011984
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/31/1997 046Control Supplement  
8/29/1997 045Control Supplement  
3/4/1997 044Control Supplement  
12/2/1996 043Control Supplement  
4/16/1996 042Manufacturing Change or Addition  
4/25/1995 041Package Change  
12/22/1994 040Control Supplement  
10/21/1994 039Labeling Revision  
4/18/1991 036Labeling Revision  
2/16/1988 035Manufacturing Change or Addition  
10/17/1988 034Labeling Revision  
2/16/1988 033Labeling Revision  
2/25/1986 031Manufacturing Change or Addition  
10/17/1988 030Labeling Revision  
12/6/1984 029Manufacturing Change or Addition  
2/12/1986 028Manufacturing Change or Addition  
6/14/1984 027Control Supplement  
9/15/1982 026Labeling Revision  
2/16/1988 025Practioner Draft Labeling  
10/27/1981 024Manufacturing Change or Addition  
10/9/1981 023Control Supplement  
12/1/1980 022Labeling Revision  
7/15/1981 021Manufacturing Change or Addition  
5/14/1982 020Manufacturing Change or Addition  
9/17/1980 019Control Supplement  
5/28/1980 018Labeling Revision  
8/26/1979 017Labeling Revision  
1/8/1980 016Labeling Revision  
5/19/1976 015Labeling Revision  
4/21/1976 014Control Supplement  
9/2/1959 000Approval  
 
There are no Therapeutic Equivalents
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