DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DELTASONE
FDA Application No:
(NDA) 009986
Active Ingredient(s):
PREDNISONE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for DELTASONE, (NDA) 009986
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/24/1993
056
Manufacturing Change or Addition
12/28/1993
055
Labeling Revision
4/6/1989
052
Manufacturing Change or Addition
5/20/1985
049
Package Change
1/9/1985
048
Labeling Revision
7/23/1979
045
Manufacturing Change or Addition
4/25/1979
044
Control Supplement
1/17/1979
043
Control Supplement
10/18/1978
042
Labeling Revision
7/20/1977
041
Control Supplement
6/21/1955
000
Approval
Therapeutic Equivalents
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