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) 089682
Active Ingredient(s):
HYDROCORTISONE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for HYDROCORTISONE, (ANDA) 089682
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/13/2001
020
Control Supplement
7/11/2001
018
Manufacturing Revision
7/11/2001
017
Labeling
7/11/2001
016
Expiration Date Change
7/11/2001
015
Packaging Addition
4/26/2001
014
Manufacturing Revision
12/29/2000
013
Control Supplement
12/30/1999
012
Chemistry
11/20/1998
011
Labeling
11/20/1998
010
Chemistry
11/20/1998
009
Chemistry
12/21/1998
008
Chemistry
9/13/1996
007
Chemistry
9/13/1996
006
Chemistry
9/13/1996
005
Chemistry
9/13/1996
004
Chemistry
11/10/1994
003
Chemistry
11/10/1994
002
Chemistry
11/10/1994
001
Labeling
3/10/1988
000
Approval
Therapeutic Equivalents
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