DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEXADROL
FDA Application No:
(NDA) 014694
Active Ingredient(s):
DEXAMETHASONE SODIUM PHOSPHATE
Company:
ORGANON USA INC
Label History
Labels are not available on this site for HEXADROL, (NDA) 014694
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/8/1995
028
Labeling Revision
8/2/1995
027
Manufacturing Change or Addition
2/28/1994
026
Manufacturing Change or Addition
3/24/1992
025
Manufacturing Change or Addition
3/28/1988
024
Labeling Revision
6/2/1987
023
Control Supplement
2/21/1985
021
Labeling Revision
1/23/1984
018
Manufacturing Change or Addition
4/27/1981
017
Manufacturing Change or Addition
4/27/1981
015
Control Supplement
12/4/1964
000
Approval
Therapeutic Equivalents
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