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) 087795
Active Ingredient(s):
HYDROCORTISONE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for HYDROCORTISONE, (ANDA) 087795
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/26/2001
022
Manufacturing Revision
12/27/2000
021
Control Supplement
12/21/1998
020
Chemistry
5/13/1997
019
Chemistry
6/28/1996
018
Chemistry
2/7/1996
017
Chemistry
10/18/1995
016
Chemistry
10/18/1995
015
Chemistry
10/18/1995
014
Chemistry
10/18/1995
013
Chemistry
10/18/1995
012
Chemistry
10/18/1995
011
Chemistry
10/18/1995
010
Chemistry
4/15/1991
009
Labeling
7/26/1989
008
Chemistry
5/12/1988
007
Chemistry
5/13/1988
005
Chemistry
6/12/1986
003
Chemistry
6/12/1986
002
Chemistry
5/3/1983
000
Approval
Therapeutic Equivalents
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