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 4,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL Bag

Label

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-125
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (Heparin) Heparin4 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
BENZYL ALCOHOL0.00004 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:52533-125-241000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/09/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: 13b971d5-b59b-4d8c-b891-533b495f3faf
Set id: 93ffe3f7-26bf-44e5-be3c-1dd58abb1066
Version: 6
Effective Time: 20141224
 
Cantrell Drug Company