Drug History: MAGNESIUM SULFATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	MAGNESIUM SULFATE
FDA Application No:	(NDA) 019316
Active Ingredient(s):	MAGNESIUM SULFATE
Company:	ABRAXIS PHARM

Label History

View the label approved on December 14, 2006 for MAGNESIUM SULFATE, (NDA) 019316

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
12/5/2006	011	Labeling Revision	Letter Label
10/28/1998	008	Labeling Revision
2/7/1996	007	Control Supplement
2/28/1995	006	Control Supplement
12/12/1994	005	Control Supplement
3/1/2000	004	Control Supplement
9/16/1991	003	Labeling Revision
11/13/1987	002	Package Change
6/19/1987	001	Package Change
9/8/1986	000	Approval

Therapeutic Equivalents