DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ACTICORT
FDA Application No:
(ANDA) 086535
Active Ingredient(s):
HYDROCORTISONE
Company:
BAKER NORTON
Label History
Labels are not available on this site for ACTICORT, (ANDA) 086535
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/22/1984
002
Chemistry
2/4/1981
000
Approval
Therapeutic Equivalents
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