Visitor Monitoring Drug History: LUPRON
 
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: LUPRON
FDA Application No: (NDA) 019010
Active Ingredient(s): LEUPROLIDE ACETATE
Company: TAP PHARM
 
Label History
 
Labels are not available on this site for LUPRON, (NDA) 019010
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/14/2007 032Labeling Revision Letter 
9/15/2005 031Labeling Revision Letter
Review 
10/18/2004 028Labeling Revision Letter 
11/25/2003 027Labeling Revision Letter 
5/16/2002 024Manufacturing Change or Addition Review 
5/16/2002 023Manufacturing Change or Addition Review 
12/21/2000 022Control Supplement  
11/22/1999 021Control Supplement  
9/25/1998 020Control Supplement  
1/8/1998 019Control Supplement  
7/7/1997 018Control Supplement  
7/7/1997 017Control Supplement  
5/28/1996 015Control Supplement  
4/24/1996 014Control Supplement  
5/9/1994 012Control Supplement  
5/9/1994 011Manufacturing Change or Addition  
6/9/1993 010Control Supplement  
7/7/1992 009Control Supplement  
10/21/1991 008Control Supplement  
5/9/1988 006Formulation Revision Review 
1/14/1987 005Control Supplement  
3/12/1987 004Labeling Revision  
1/19/1988 003Control Supplement  
7/10/1986 002Control Supplement  
4/9/1985 000Approval  
 
Therapeutic Equivalents
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