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 0.45% Sodium Chloride 500 mL Bag

Label

HEPARIN SODIUM 
heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-216
Route of Administration INTRAVENOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 50 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride (UNII: 451W47IQ8X) 4.5 mg  in 1 mL
BENZYL ALCOHOL (UNII: LKG8494WBH) 0.0001 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:52533-216-40 500 mL in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 12/21/2012
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2014
Document Id: b85145ea-46ad-49da-bf4e-641316e7fcaa
Set id: fda3f337-deab-40f3-bc0d-0c08baeb8a2d
Version: 3
Effective Time: 20141224
 
Cantrell Drug Company