DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SODIUM ACETATE IN PLASTIC CONTAINER
FDA Application No:
(NDA) 018893
Active Ingredient(s):
SODIUM ACETATE, ANHYDROUS
Company:
HOSPIRA
Label History
Labels are not available on this site for SODIUM ACETATE IN PLASTIC CONTAINER, (NDA) 018893
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/3/2003
017
Control Supplement
Letter
2/16/2001
016
Package Change
8/31/1999
015
Package Change
1/22/1999
014
Control Supplement
6/15/2000
013
Labeling Revision
5/5/1998
012
Labeling Revision
8/29/1996
011
Control Supplement
1/17/1997
010
Control Supplement
11/17/1988
008
Control Supplement
12/11/1987
007
Control Supplement
7/24/1986
006
Control Supplement
5/14/1985
005
Control Supplement
10/22/1984
004
Control Supplement
3/15/1985
003
Control Supplement
1/17/1984
002
Control Supplement
5/4/1983
000
Approval
There are no Therapeutic Equivalents
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