DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VANCENASE
FDA Application No:
(NDA) 018521
Active Ingredient(s):
BECLOMETHASONE DIPROPIONATE
Company:
SCHERING
Label History
Labels are not available on this site for VANCENASE, (NDA) 018521
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/30/2000
032
Control Supplement
7/26/2000
031
Control Supplement
3/11/1999
029
Control Supplement
8/3/1995
026
Control Supplement
3/3/1997
025
Labeling Revision
2/3/1997
024
Labeling Revision
12/15/1988
023
Labeling Revision
8/2/1988
021
Manufacturing Change or Addition
8/4/1988
020
Labeling Revision
9/24/1987
019
Manufacturing Change or Addition
2/1/1988
018
Control Supplement
7/8/1986
017
Control Supplement
3/6/1986
016
Manufacturing Change or Addition
2/24/1986
015
Labeling Revision
2/24/1986
014
Control Supplement
11/2/1985
013
Labeling Revision
1/2/1985
012
Control Supplement
11/2/1985
011
General Efficacy (MarkIV)
2/21/1985
010
Control Supplement
12/17/1984
007
Control Supplement
5/9/1988
006
Labeling Revision
2/4/1982
005
Control Supplement
2/4/1982
004
Control Supplement
12/3/1981
003
Control Supplement
11/6/1981
002
Labeling Revision
11/6/1981
001
Control Supplement
9/24/1981
000
Approval
Therapeutic Equivalents
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