Drug History: MANNITOL 20% IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Label and Approval History

Drug Name:	MANNITOL 20% IN PLASTIC CONTAINER
FDA Application No:	(NDA) 019603
Active Ingredient(s):	MANNITOL
Company:	HOSPIRA

Label History

Labels are not available on this site for MANNITOL 20 IN PLASTIC CONTAINER, (NDA) 019603

Approval History

Action Date	Supplement Number	Approval Type
7/10/2000	018	Control Supplement
12/1/1998	017	Chemistry
6/11/1997	016	Chemistry
8/6/1996	015	Chemistry
3/4/1996	014	Chemistry
8/14/1995	013	Chemistry
8/29/1996	012	Chemistry
8/27/1996	011	Chemistry
8/25/1994	010	Labeling
1/28/1992	008	Chemistry
9/10/1991	007	Chemistry
6/4/1990	005	Chemistry
1/11/1990	004	Chemistry
2/22/1990	003	Chemistry
1/8/1990	002	Labeling
1/8/1990	001	Chemistry
1/8/1987	000	Approval