Drug History: M.V.I. PEDIATRIC

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:	M.V.I. PEDIATRIC
FDA Application No:	(NDA) 018920
Active Ingredient(s):	ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PHYTONADIONE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E
Company:	HOSPIRA

Label History

View the label approved on July 8, 2002 for M.V.I. PEDIATRIC, (NDA) 018920

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
11/30/2001	025	Manufacturing Change or Addition
7/9/2002	024	Labeling Revision	Letter Label
6/5/2001	023	Manufacturing Change or Addition
11/2/2000	022	Control Supplement
9/21/2000	021	Control Supplement
9/21/2000	020	Labeling Revision
6/5/2001	019	Control Supplement
4/12/2000	018	Control Supplement
8/13/1999	017	Control Supplement
12/16/1998	016	Control Supplement
3/25/1998	015	Labeling Revision
4/9/1996	014	Labeling Revision
1/19/1996	013	Control Supplement
10/18/1995	011	Control Supplement
5/26/1995	010	Control Supplement
2/24/1993	009	Package Change
2/22/1993	008	Labeling Revision
4/19/1991	007	Labeling Revision
6/22/1989	006	Labeling Revision
12/8/1986	005	Control Supplement
12/3/1986	004	Labeling Revision
5/15/1985	003	Labeling Revision
7/6/1984	002	Labeling Revision
7/6/1984	001	Labeling Revision
4/6/1983	000	Approval

There are no Therapeutic Equivalents