Drug History: M.V.I.-12 (WITHOUT VITAMIN K)

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	M.V.I.-12 (WITHOUT VITAMIN K)
FDA Application No:	(NDA) 008809
Active Ingredient(s):	ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E
Company:	HOSPIRA

Label History

View the label approved on September 10, 2004 for M.V.I.12 (WITHOUT VITAMIN K), (NDA) 008809

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
9/9/2004	054	New or Modified Indication	Letter Label
4/22/2004	052	Formulation Revision	Letter Label
11/14/2002	048	Control Supplement
6/4/2002	047	Control Supplement
6/4/2002	046	Labeling Revision	Letter
4/17/2001	045	Manufacturing Change or Addition
4/17/2001	044	Manufacturing Change or Addition
4/10/2001	043	Manufacturing Change or Addition
8/2/1999	042	Control Supplement
5/25/1999	041	Control Supplement
11/18/1998	040	Control Supplement
5/12/1998	039	Package Change
12/31/1997	038	Package Change
3/30/1998	037	Manufacturing Change or Addition
9/22/1997	036	Control Supplement
2/13/1997	035	Control Supplement
1/19/1996	033	Control Supplement
10/27/1995	031	Control Supplement
5/26/1995	030	Control Supplement
2/24/1993	029	Control Supplement
2/3/1993	028	Package Change
2/2/1993	027	Package Change
4/19/1991	025	Labeling Revision
12/7/1990	024	Package Change
6/22/1989	023	Labeling Revision
8/8/1985	021	Labeling Revision
4/24/1985	020	Package Change
4/25/1985	019	Package Change
9/20/1984	018	Labeling Revision
2/20/1953	000	Approval

There are no Therapeutic Equivalents