DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ELOCON
FDA Application No:
(NDA) 019796
Active Ingredient(s):
MOMETASONE FUROATE
Company:
SCHERING
Label History
View the
label approved on September 15, 2005
for ELOCON, (NDA) 019796
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 Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/9/2005
020
Labeling Revision
Letter
Label
7/17/2002
015
Patient Population Altered
Letter
Label
7/13/2001
014
Control Supplement
9/7/2000
013
Package Change
5/14/1999
012
Control Supplement
12/28/1998
011
Manufacturing Change or Addition
11/2/1998
010
Control Supplement
6/5/1998
009
Manufacturing Change or Addition
7/17/2002
008
Labeling Revision
Letter
Label
4/16/1996
007
Control Supplement
1/25/1996
006
Manufacturing Change or Addition
3/11/1992
005
Package Change
9/25/1991
004
Control Supplement
6/13/1989
001
Package Change
3/30/1989
000
Approval
Therapeutic Equivalents
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