MAGNESIUM SULFATE INJECTION, SOLUTION [CANTRELL DRUG COMPANY]

MAGNESIUM SULFATE INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
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NDC	52533-099-29
Set ID	88f80e1e-d6e3-4789-abe1-f62db9ca366b
Category	HUMAN PRESCRIPTION DRUG LABEL
Packager	Cantrell Drug Company
Generic Name
Product Class
Product Number
Application Number

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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

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

Ingredient Name	Strength
Inactive Ingredients
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

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

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

Labeler - Cantrell Drug Company (035545763)

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