MAGNESIUM SULFATE injection, solution

Magnesium Sulfate by

Drug Labeling and Warnings

Magnesium Sulfate by is a Prescription medication manufactured, distributed, or labeled by Cantrell Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Label

SPL UNCLASSIFIED SECTION

INGREDIENTS AND APPEARANCE

MAGNESIUM SULFATE 
magnesium sulfate injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 52533-099
Route of Administration	INTRAVENOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNESIUM SULFATE (UNII: DE08037SAB) (Magnesium Cation - UNII:T6V3LHY838)	MAGNESIUM SULFATE	20 g  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)	3 g  in 500 mL
SODIUM LACTATE (UNII: TU7HW0W0QT)	1.55 g  in 500 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10)	0.15 g  in 500 mL
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)	0.1 g  in 500 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52533-099-29	500 mL in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/21/2011

Labeler - Cantrell Drug Company (035545763)