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

MM1

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:52533-104
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HEPARIN SODIUM (HEPARIN) HEPARIN10 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Sodium Chloride9 mg  in 1 mL
BENZYL ALCOHOL9 mg  in 1 mL
Water 
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID 
May containSODIUM HYDROXIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-104-703 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: 9d75afcc-097c-434a-9920-2fbbf53eac48
Set id: ff3ec64a-280a-4978-9c66-2cbc768a7484
Version: 8
Effective Time: 20140502
 
Cantrell Drug Company