DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEDROL ACETATE
FDA Application No:
(NDA) 012421
Active Ingredient(s):
METHYLPREDNISOLONE ACETATE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for MEDROL ACETATE, (NDA) 012421
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/2/1982
022
Labeling Revision
12/28/1981
021
Formulation Revision
2/29/1980
019
Labeling Revision
11/11/1977
018
Control Supplement
2/27/1976
017
Labeling Revision
6/21/1960
000
Approval
There are no Therapeutic Equivalents
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