DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LUPRON
FDA Application No:
(NDA) 019943
Active Ingredient(s):
LEUPROLIDE ACETATE
Company:
TAP PHARM
Label History
Labels are not available on this site for LUPRON, (NDA) 019943
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/15/2005
024
Labeling Revision
Letter
Review
9/15/2005
022
Control Supplement
Letter
Review
1/12/2004
021
Labeling Revision
Letter
9/20/2002
019
Control Supplement
1/15/2004
018
Labeling Revision
Letter
5/23/2002
017
Control Supplement
2/21/2002
016
Control Supplement
11/14/2001
015
Labeling Revision
3/1/2001
014
Labeling Revision
1/24/2001
013
Control Supplement
5/12/2000
012
Control Supplement
5/11/2000
011
Control Supplement
8/13/1999
010
Manufacturing Change or Addition
Review
6/30/1998
009
Control Supplement
6/27/1997
007
Control Supplement
9/12/1996
006
Labeling Revision
8/11/1995
004
Control Supplement
10/26/1995
003
Package Change
Review
12/12/1995
002
Labeling Revision
9/22/1995
001
Manufacturing Change or Addition
3/30/1995
000
Approval
Review
There are no Therapeutic Equivalents
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