Visitor Monitoring Drug History: HEXALEN
 
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: HEXALEN
FDA Application No: (NDA) 019926
Active Ingredient(s): ALTRETAMINE
Company: MGI PHARMA INC
 
Label History
 
View the label approved on December 26, 1990 for HEXALEN, (NDA) 019926


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/11/2001 017Control Supplement  
10/19/1999 016Control Supplement  
4/11/1997 015Manufacturing Change or Addition  
7/11/1995 014Control Supplement  
6/23/1995 013Package Change  
7/26/1994 012Control Supplement  
3/12/1993 011Manufacturing Change or Addition  
2/10/1993 010Labeling Revision  
5/29/1992 009Control Supplement  
3/19/1992 008Control Supplement  
10/22/1991 007Manufacturing Change or Addition  
9/20/1991 006Control Supplement  
1/14/1993 005Control Supplement  
4/26/1991 004Control Supplement  
1/14/1993 003Control Supplement  
3/14/1991 001Control Supplement  
12/26/1990 000Approval Label 
 
There are no Therapeutic Equivalents
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