DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MAGNACORT
FDA Application No:
(NDA) 010554
Active Ingredient(s):
HYDROCORTAMATE HYDROCHLORIDE
Company:
PFIZER
Label History
Labels are not available on this site for MAGNACORT, (NDA) 010554
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/15/1956
000
Approval
There are no Therapeutic Equivalents
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