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.


Heparin Sodium 25,000 USP Units Added to 0.45% Sodium Chloride 500 mL Bag


heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-216
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (Heparin) Heparin50 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride4.5 mg  in 1 mL
BENZYL ALCOHOL0.0001 mL  in 1 mL
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-216-40500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/21/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 5/2013
Document Id: 97e3c4de-29ab-4d25-82d8-200fc292f547
Set id: fda3f337-deab-40f3-bc0d-0c08baeb8a2d
Version: 2
Effective Time: 20130501
Cantrell Drug Company