Visitor Monitoring Drug History: DEPO-MEDROL
 
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Label and Approval History

Drug Name: DEPO-MEDROL
FDA Application No: (NDA) 011757
Active Ingredient(s): METHYLPREDNISOLONE ACETATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for DEPOMEDROL, (NDA) 011757
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/22/2002 079Control Supplement  
4/4/2000 078Manufacturing Change or Addition  
1/24/1995 075Package Change  
1/7/1994 072Manufacturing Change or Addition  
12/28/1993 070Package Change  
11/15/1990 064Formulation Revision  
12/14/1989 063Labeling Revision  
5/12/1986 060Labeling Revision  
1/5/1989 059Package Change  
3/9/1983 058Labeling Revision  
3/9/1983 057Labeling Revision  
5/12/1986 055Labeling Revision  
7/29/1980 054Expiration Date Change  
5/12/1986 053Labeling Revision  
7/12/1978 052Labeling Revision  
2/17/1981 050Control Supplement  
5/27/1959 000Approval  
 
Therapeutic Equivalents
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