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 5,000 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:52533-098
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin10 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
BENZYL ALCOHOL (UNII: LKG8494WBH) 0.001 mL  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:52533-098-30500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/30/2011
Labeler - Cantrell Drug Company (035545763)
Establishment
NameAddressID/FEIBusiness Operations
Cantrell Drug Company035545763manufacture(52533-098) , human drug compounding outsourcing facility(52533-098) (No intent to compound 506E (drug shortage) drugs), (Not compounding from bulk ingredient)

Revised: 12/2014
Document Id: 7938e6ac-68cd-41cb-b4e7-d53b1c624b7b
Set id: 69333d0f-8bee-4975-9d3c-0fa7027ddfea
Version: 5
Effective Time: 20141224
 
Cantrell Drug Company