Visitor Monitoring Drug History: CORTEF
 
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Label and Approval History

Drug Name: CORTEF
FDA Application No: (NDA) 008697
Active Ingredient(s): HYDROCORTISONE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for CORTEF, (NDA) 008697
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/16/2001 025Manufacturing Change or Addition  
12/28/1993 021Labeling Revision  
12/8/1993 020Manufacturing Change or Addition  
3/9/1983 016Control Supplement  
2/8/1978 014Labeling Revision  
12/15/1952 000Approval  
 
Therapeutic Equivalents
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