DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VALISONE
FDA Application No:
(NDA) 016740
Active Ingredient(s):
BETAMETHASONE VALERATE
Company:
SCHERING
Label History
Labels are not available on this site for VALISONE, (NDA) 016740
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/8/1991
018
Control Supplement
9/12/1986
017
Manufacturing Change or Addition
5/20/1986
016
Control Supplement
1/7/1986
015
Control Supplement
4/23/1986
014
Expiration Date Change
4/16/1982
013
Manufacturing Change or Addition
9/15/1981
012
Manufacturing Change or Addition
9/15/1981
011
Control Supplement
12/22/1982
010
Practioner Draft Labeling
12/26/1979
009
Distributor
5/31/1979
008
Control Supplement
6/3/1980
007
Control Supplement
4/17/1980
006
Labeling Revision
9/6/1977
005
Package Change
5/31/1974
004
Supplement
2/17/1969
000
Approval
Therapeutic Equivalents
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