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) 019543
Active Ingredient(s):
MOMETASONE FUROATE
Company:
SCHERING
Label History
View the
label approved on December 15, 2002
for ELOCON, (NDA) 019543
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
12/15/2002
014
Labeling Revision
Letter
Label
7/17/2002
013
Patient Population Altered
Letter
Label
2/27/2002
012
Control Supplement
7/17/2002
011
Labeling Revision
Letter
Label
1/20/2000
010
Control Supplement
11/10/1998
009
Package Change
12/28/1998
008
Manufacturing Change or Addition
6/9/1998
007
Manufacturing Change or Addition
3/7/1997
006
Package Change
4/16/1996
005
Control Supplement
9/25/1991
004
Control Supplement
10/3/1995
003
Patient Population Altered
10/29/1987
001
Manufacturing Change or Addition
4/30/1987
000
Approval
Therapeutic Equivalents
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