Visitor Monitoring Drug History: ELIGARD
 
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Label and Approval History

Drug Name: ELIGARD
FDA Application No: (NDA) 021731
Active Ingredient(s): LEUPROLIDE ACETATE
Company: QLT USA
 
Label History
 
Labels are not available on this site for ELIGARD, (NDA) 021731
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/29/2006 004Package Change Letter 
12/14/2004 000Approval Review 
 
There are no Therapeutic Equivalents
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