Visitor Monitoring Drug History: MEGACE
 
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: MEGACE
FDA Application No: (NDA) 020264
Active Ingredient(s): MEGESTROL ACETATE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for MEGACE, (NDA) 020264
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/1/2003 011Labeling Revision Letter 
4/9/2002 009Labeling Revision Letter 
7/27/2000 008Control Supplement  
6/25/1998 006Manufacturing Change or Addition  
3/24/1998 005Manufacturing Change or Addition  
8/8/1997 004Labeling Revision  
10/22/1996 003Labeling Revision  
7/29/1994 002Control Supplement  
11/4/1994 001Labeling Revision  
9/10/1993 000Approval  
 
Therapeutic Equivalents
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