HEPARIN SODIUM - heparin sodium injection, solution 
Cantrell Drug Company

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Heparin Sodium 20,000 USP Units Added to 5% Dextrose 500 mL Bag

MM1

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-215
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin40 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DEXTROSE (UNII: IY9XDZ35W2) 50 mg  in 1 mL
BENZYL ALCOHOL (UNII: LKG8494WBH) 0.00008 mL  in 1 mL
Water (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID (UNII: QTT17582CB)  
May containSODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-215-32500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/08/2014
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: f80df7a0-ec3e-4736-bfe3-fddaddae0812
Set id: f23a3afd-b4b6-4446-bd2c-74a2eea7f111
Version: 2
Effective Time: 20141224
 
Cantrell Drug Company