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

Label

HEPARIN SODIUM 
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
Water 
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID 
May containSODIUM HYDROXIDE 
Packaging
#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: 12/2014
Document Id: b85145ea-46ad-49da-bf4e-641316e7fcaa
Set id: fda3f337-deab-40f3-bc0d-0c08baeb8a2d
Version: 3
Effective Time: 20141224
 
Cantrell Drug Company