DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYDROCORTISONE
FDA Application No:
(ANDA) 087317
Active Ingredient(s):
HYDROCORTISONE
Company:
ALPHARMA US PHARMS
Label History
Labels are not available on this site for HYDROCORTISONE, (ANDA) 087317
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/8/1989
004
Chemistry
2/4/1987
002
Chemistry
4/1/1986
001
Chemistry
Therapeutic Equivalents
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