DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DEXAMETHASONE
FDA Application No:
(ANDA) 087702
Active Ingredient(s):
DEXAMETHASONE SODIUM PHOSPHATE
Company:
BAXTER HLTHCARE
Label History
Labels are not available on this site for DEXAMETHASONE, (ANDA) 087702
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/7/2003
029
Expiration Date Change
9/5/2001
028
Control Supplement
7/11/2000
027
Control Supplement
9/7/1999
026
Chemistry
12/1/1998
025
Chemistry
6/12/1998
022
Chemistry
5/7/1998
021
Chemistry
2/15/1995
020
Labeling
4/19/1994
019
Chemistry
1/27/1994
018
Labeling in Effect
10/28/1991
017
Labeling
6/12/1991
016
Labeling
1/14/1992
014
Chemistry
9/21/1989
013
Labeling
5/26/1989
012
Labeling
5/26/1989
011
Labeling
2/7/1989
010
Labeling
4/2/1987
009
Chemistry
3/21/1988
006
Chemistry
3/21/1988
005
Chemistry
3/21/1988
004
Chemistry
11/27/1984
003
Chemistry
1/31/1983
002
Chemistry
1/31/1983
001
Chemistry
9/7/1982
000
Approval
Therapeutic Equivalents
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