DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYTONE
FDA Application No:
(ANDA) 080473
Active Ingredient(s):
HYDROCORTISONE
Company:
SANOFI AVENTIS US
Label History
Labels are not available on this site for HYTONE, (ANDA) 080473
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/27/2002
020
Facility Addition
3/4/1999
019
Chemistry
1/20/1998
018
Chemistry
11/30/1993
017
Chemistry
1/27/1992
016
Chemistry
1/27/1992
015
Chemistry
11/2/1983
012
Chemistry
7/8/1983
011
Chemistry
11/30/1982
009
Chemistry
11/30/1982
008
Chemistry
1/11/1983
007
Chemistry
9/25/1972
000
Approval
Therapeutic Equivalents
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