DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DECASPRAY
FDA Application No:
(NDA) 012731
Active Ingredient(s):
DEXAMETHASONE
Company:
MERCK
Label History
Labels are not available on this site for DECASPRAY, (NDA) 012731
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/29/1991
015
Control Supplement
7/8/1988
012
Manufacturing Change or Addition
9/5/1984
011
Labeling Revision
9/24/1984
010
Manufacturing Change or Addition
2/2/1979
007
Formulation Revision
3/29/1961
000
Approval
There are no Therapeutic Equivalents
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