Drug History: HEPARIN SODIUM 5,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Label and Approval History

Drug Name:	HEPARIN SODIUM 5,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:	(NDA) 018609
Active Ingredient(s):	HEPARIN SODIUM
Company:	BAXTER HLTHCARE

Label History

View the label approved on April 14, 2003 for HEPARIN SODIUM 5,000 UNITS AND SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 018609

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
8/14/2001	037	Control Supplement
11/23/1999	036	Package Change
8/21/2001	035	Labeling Revision	Label
6/1/1999	034	Manufacturing Change or Addition
8/21/2001	033	Labeling Revision	Label
5/20/1997	032	Package Change
9/17/1996	031	Labeling Revision
3/10/1994	030	Control Supplement
9/14/1994	029	Manufacturing Change or Addition
4/15/1993	027	Manufacturing Change or Addition
3/4/1991	025	Control Supplement
7/26/1990	024	Control Supplement
2/1/1991	023	Package Change
8/24/1989	022	Control Supplement
11/8/1989	021	Labeling Revision
4/29/1987	020	Package Change
12/1/1986	019	Control Supplement
12/1/1986	018	Control Supplement
9/20/1985	017	Control Supplement
9/20/1985	016	Package Change
11/8/1989	015	Labeling Revision
10/16/1984	014	Control Supplement
8/3/1984	013	Manufacturing Change or Addition
2/28/1984	012	Control Supplement
3/6/1984	011	Labeling Revision
11/8/1989	010	Practioner Draft Labeling
3/6/1984	009	Control Supplement
3/6/1984	008	Package Change
3/6/1984	004	Package Change
8/9/1982	003	Package Change
8/9/1982	002	Control Supplement
6/29/1982	001	Expiration Date Change
4/28/1982	000	Approval

There are no Therapeutic Equivalents