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 1,000 USP Units Added to 0.9% Sodium Chloride 500 mL Bag

Label

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-138
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin2 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 mg  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:52533-138-30500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/29/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: 70b5656c-8fe5-4474-a6fd-e6e4be49a644
Set id: 73444d4d-81a2-4cdb-a7f9-ee0067463fa2
Version: 4
Effective Time: 20141224
 
Cantrell Drug Company