Label: MAGNESIUM SULFATE injection, solution
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Contains inactivated NDC Code(s)
NDC Code(s): 52533-107-38 - 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:52533-107 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 250 mL Inactive Ingredients Ingredient Name Strength Dextrose (UNII: IY9XDZ35W2) 12.5 g in 250 mL Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52533-107-38 250 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/25/2011 Labeler - Cantrell Drug Company (035545763)
