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 10 USP Units/mL in 0.9% Sodium Chloride 3 mL Syringe

MM1

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-104
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) 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:52533-104-703 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/07/2011
Labeler - Cantrell Drug Company (035545763)

Revised: 5/2014
Document Id: d79d1eb4-bd87-4879-aa42-c571f2040ccb
Set id: ff3ec64a-280a-4978-9c66-2cbc768a7484
Version: 9
Effective Time: 20140528
 
Cantrell Drug Company