Label: HEPARIN SODIUM injection, solution
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Contains inactivated NDC Code(s)
NDC Code(s): 52533-106-32 - 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 December 24, 2014
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INGREDIENTS AND APPEARANCE
HEPARIN SODIUM
heparin sodium injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-106 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 50 [USP'U] in 1 mL Inactive Ingredients Ingredient Name Strength DEXTROSE (UNII: IY9XDZ35W2) 50 mg in 1 mL BENZYL ALCOHOL (UNII: LKG8494WBH) 0.0001 mL in 1 mL Water (UNII: 059QF0KO0R) Other Ingredients Ingredient Kind Ingredient Name Quantity May contain HYDROCHLORIC ACID (UNII: QTT17582CB) May contain SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52533-106-32 500 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/09/2012 Labeler - Cantrell Drug Company (035545763)
