Visitor Monitoring Drug History: MEDROL
 
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: MEDROL
FDA Application No: (NDA) 011153
Active Ingredient(s): METHYLPREDNISOLONE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for MEDROL, (NDA) 011153
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/25/2002 059Manufacturing Change or Addition  
12/1/1999 058Package Change  
1/28/1993 052Manufacturing Change or Addition  
12/28/1993 051Labeling Revision  
1/5/1989 049Manufacturing Change or Addition  
2/24/1987 047Control Supplement  
3/9/1983 046Labeling Revision  
10/8/1980 044Formulation Revision  
4/14/1980 043Labeling Revision  
4/5/1979 042Manufacturing Change or Addition  
4/11/1978 041Labeling Revision  
5/30/1979 040Formulation Revision  
4/5/1979 039Formulation Revision  
9/10/1976 037Control Supplement  
10/24/1957 000Approval  
 
Therapeutic Equivalents
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