Drug History: SODIUM CHLORIDE 5% IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	SODIUM CHLORIDE 5% IN PLASTIC CONTAINER
FDA Application No:	(NDA) 019022
Active Ingredient(s):	SODIUM CHLORIDE
Company:	BAXTER HLTHCARE

Label History

View the label approved on August 31, 2005 for SODIUM CHLORIDE 5 IN PLASTIC CONTAINER, (NDA) 019022

To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
8/26/2005	022	Package Change	Letter Label
6/9/2005	021	Labeling Revision	Letter Label
8/14/2001	019	Manufacturing Change or Addition
11/24/1999	018	Manufacturing Change or Addition
4/3/2002	017	Labeling Revision	Letter
4/29/1997	016	Package Change
2/18/1994	015	Control Supplement
9/30/1994	014	Control Supplement
4/29/1991	012	Control Supplement
3/26/1991	011	Control Supplement
5/24/1990	010	Control Supplement
2/15/1991	009	Control Supplement
7/26/1989	008	Control Supplement
5/28/1987	006	Control Supplement
4/26/1985	005	Control Supplement
1/26/1985	004	Labeling Revision
6/13/1985	003	Control Supplement
9/22/1984	002	Control Supplement
12/6/1984	001	Control Supplement
11/1/1983	000	Approval

Therapeutic Equivalents