Visitor Monitoring Drug History: CORTEF
 
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: CORTEF
FDA Application No: (NDA) 009900
Active Ingredient(s): HYDROCORTISONE CYPIONATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for CORTEF, (NDA) 009900
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/1/1997 027Manufacturing Change or Addition  
12/28/1993 023Labeling Revision  
8/29/1990 022Formulation Revision  
6/30/1982 018Control Supplement  
6/4/1979 016Labeling Revision  
5/10/1955 000Approval  
 
There are no Therapeutic Equivalents
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