Visitor Monitoring Drug History: CORTEF ACETATE
 
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Label and Approval History

Drug Name: CORTEF ACETATE
FDA Application No: (NDA) 009378
Active Ingredient(s): HYDROCORTISONE ACETATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for CORTEF ACETATE, (NDA) 009378
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/22/1989 020Labeling Revision  
11/10/1981 019Labeling Revision  
9/27/1979 017Package Change  
3/7/1978 016Labeling Revision  
3/15/1977 015Manufacturing Change or Addition  
5/5/1977 014Labeling Revision  
 
Therapeutic Equivalents
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