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 2,500 USP Units Added to 4.5% Sodium Chloride 500 mL Bag

Label

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-096
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (Heparin) Heparin5 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE4.5 mg  in 1 mL
BENZYL ALCOHOL0.00005 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:52533-096-40500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/18/2011
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: f9e573f1-53bc-4cb8-82ed-d7ee761970ca
Set id: 4334dd71-66f8-4e7f-9a41-53a9f81cbebc
Version: 5
Effective Time: 20141224
 
Cantrell Drug Company