Label: MAGNESIUM SULFATE injection, solution
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Contains inactivated NDC Code(s)
NDC Code(s): 52533-099-29 - Packager: Cantrell Drug Company
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 21, 2012
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INGREDIENTS AND APPEARANCE
MAGNESIUM SULFATE
magnesium sulfate injection, solutionProduct 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)
