Visitor Monitoring Drug History: CORTEF ACETATE
 
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Label and Approval History

Drug Name: CORTEF ACETATE
FDA Application No: (NDA) 008917
Active Ingredient(s): HYDROCORTISONE ACETATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for CORTEF ACETATE, (NDA) 008917
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/5/1990 021Control Supplement  
4/28/1987 019Package Change  
4/28/1987 018Formulation Revision  
10/14/1982 017Practioner Draft Labeling  
3/19/1980 016Labeling Revision  
10/11/1977 014Control Supplement  
2/10/1977 013Control Supplement  
10/12/1976 012Control Supplement  
6/3/1976 011Labeling Revision  
7/28/1953 000Approval  
 
There are no Therapeutic Equivalents
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