DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISONE
FDA Application No:
(ANDA) 089983
Active Ingredient(s):
PREDNISONE
Company:
SANDOZ
Label History
Labels are not available on this site for PREDNISONE, (ANDA) 089983
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/9/2001
005
Control Supplement
1/24/1994
004
Chemistry
10/15/1992
003
Chemistry
8/3/1989
001
Labeling
1/12/1989
000
Approval
Therapeutic Equivalents
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