Visitor Monitoring Drug History: NEO-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: NEO-CORTEF
FDA Application No: (ANDA) 060751
Active Ingredient(s): HYDROCORTISONE ACETATE; NEOMYCIN SULFATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for NEOCORTEF, (ANDA) 060751
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/22/1993 008Chemistry in Effect  
4/22/1991 007Chemistry  
6/23/1992 006Chemistry  
3/4/1991 005Chemistry  
5/18/1965 000Approval  
 
There are no Therapeutic Equivalents
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