Heparin Sodium

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.

Label
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• WARNINGS AND PRECAUTIONS

Outsourced Compounded Drug. Not for Resale. Hospital/Office Use Only.

• ADVERSE EVENTS

To facilitate Adverse Event Reporting: www.fda.gov/medwatch or 1-800-FDA-1088.

• HOW SUPPLIED

Contains 25,000 USP Units of Heparin Sodium in 0.45% Sodium Chloride in a 250 mL Single-Dose Bag. Volume & Concentration exlude additive & manufacturer overfill.

This product is Sterile, Nonpyrogenic, and Latex Free.

• INGREDIENTS

Each 1 mL contains contains Heparin Sodium 100 USP Units, Sodium Chloride 4.5 mg, Benzyl Alcohol 0.0002 mL. May contain Hydrochloric Acid and/or Sodium Hydroxide for pH adjustment.

• STORAGE AND HANDLING

Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature].

• DOSAGE AND ADMINISTRATION.

FOR INTRAVENOUS USE.

Rx Only

Rev. 05/15

CANTRELL DRUG COMPANY

LITTLE ROCK, AR 72207

HEPARIN SODIUM
heparin sodium injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-179
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Heparin Sodium (Heparin) Heparin 100 [USP’U] in 1 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride 4.5 mg in 1 mL
BENZYL ALCOHOL 0.0002 mL in 1 mL
Water
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52533-179-18 250 mL in 1 BAG None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/15/2015
Labeler — Cantrell Drug Company (035545763)

Revised: 05/2015 Cantrell Drug Company

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