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) 012071
Active Ingredient(s): DEXAMETHASONE SODIUM PHOSPHATE
Company: MERCK
 
Label History
 
Labels are not available on this site for DECADRON, (NDA) 012071
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/18/2000 053Control Supplement  
10/22/1997 049Control Supplement  
9/9/1997 047Control Supplement  
2/17/1999 046Control Supplement  
3/1/1996 043Manufacturing Change or Addition  
8/26/1993 039Labeling Revision  
12/11/1989 038Package Change  
3/8/1985 031Labeling Revision  
6/25/1984 030Manufacturing Change or Addition  
8/15/1979 026Labeling Revision  
10/18/1978 025Labeling Revision  
2/5/1981 023Package Change  
10/6/1959 000Approval  
 
Therapeutic Equivalents
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