DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEDROL
FDA Application No:
(NDA) 018102
Active Ingredient(s):
METHYLPREDNISOLONE ACETATE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for MEDROL, (NDA) 018102
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/19/1982
004
Control Supplement
4/1/1981
002
Formulation Revision
12/21/1977
000
Approval
There are no Therapeutic Equivalents
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