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 25,000 USP Units Added to 5% Dextrose 250 mL Bag

Label

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-142
Route of Administration INTRAVENOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 100 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
DEXTROSE (UNII: IY9XDZ35W2) 50 mg  in 1 mL
BENZYL ALCOHOL (UNII: LKG8494WBH) 0.0002 mL  in 1 mL
Water (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient Kind Ingredient Name Quantity
May contain HYDROCHLORIC ACID (UNII: QTT17582CB)  
May contain SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52533-142-38 250 mL in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 08/29/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: 06a6c4e5-41c6-41af-bfe1-520f7e0e9420
Set id: 5371085b-6450-4a7a-a0dc-e68cabb0c8c8
Version: 7
Effective Time: 20141224
 
Cantrell Drug Company