DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISOLONE
FDA Application No:
(ANDA) 080339
Active Ingredient(s):
PREDNISOLONE
Company:
SANDOZ
Label History
Labels are not available on this site for PREDNISOLONE, (ANDA) 080339
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/4/1994
049
Labeling
1/24/1994
048
Chemistry
5/10/1990
047
Labeling
11/2/1989
046
Labeling in Effect
7/12/1989
045
Labeling
4/7/1988
044
Chemistry
4/7/1988
043
Chemistry
8/9/1985
042
Chemistry
8/9/1985
041
Chemistry
8/9/1985
040
Chemistry
11/5/1982
036
Chemistry
11/5/1982
035
Chemistry
10/13/1982
034
Chemistry
9/7/1982
033
Chemistry
9/7/1982
032
Chemistry
9/6/1972
000
Approval
Therapeutic Equivalents
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