DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(ANDA) 088912
Active Ingredient(s):
SODIUM CHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (ANDA) 088912
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/21/2007
024
Facility Addition
5/13/2002
022
Manufacturing Revision
6/8/1998
021
Chemistry
2/2/1993
020
Labeling
11/2/1992
019
Labeling in Effect
8/11/1992
018
Labeling
11/15/1994
017
Chemistry in Effect
11/15/1994
016
Chemistry
9/28/1987
012
Chemistry
9/28/1987
011
Chemistry
6/8/1987
010
Chemistry
1/14/1986
008
Chemistry
11/29/1985
005
Chemistry
11/29/1985
003
Chemistry
1/10/1985
000
Approval
Therapeutic Equivalents
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