Sodium Chloride description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Sodium Chloride

Hospira, Inc.

Preservative-Free 0.9% Sodium Chloride Injection, USP


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Rx only

SODIUM CHLORIDE DESCRIPTION

0.9% Sodium Chloride Injection, USP in Carpuject ™ sterile cartridge unit (2 mL, 3 mL, and 5 mL fill), is a sterile aqueous isotonic solution of sodium chloride in Water for Injection. The total osmolar concentration of the solution is 0.31 mOsm/mL. Each mL contains 9 mg of sodium chloride.

CLINICAL PHARMACOLOGY

0.9% Sodium Chloride Injection, USP is a sterile aqueous vehicle having approximately the same osmotic pressure and composition as extracellular fluids. It is nonirritating to tissues.

SODIUM CHLORIDE INDICATIONS AND USAGE

For use as a sterile isotonic vehicle for diluting or dissolving compatible parenteral medications.

PRECAUTIONS

If compatibility is in doubt, consult the appropriate specialized literature before mixing with any drug product. Do not administer if a precipitate appears, if solution is cloudy or hazy, or if any other visible change occurs upon mixing.

For single use only. Discard unused solution.

SODIUM CHLORIDE DOSAGE AND ADMINISTRATION

Use in accord with any warnings or precautions appropriate to the medication being administered.

HOW SUPPLIED

NDC No.

Container

Fill

Quantity

0409-1918-32

Carpuject™ with Luer Lock

2 mL fill in 2 mL cartridge

bins of 50

0409-1918-33

Carpuject™ with Luer Lock

3 mL fill in 5 mL cartridge

bins of 25

0409-1918-35

Carpuject™ with Luer Lock

5 mL fill in 5 mL cartridge

bins of 25

Do not use if solution is discolored or contains a precipitate.

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

Do not freeze.

Revised: November, 2009

Printed in USA

EN-2305

Hospira, Inc., Lake Forest, IL 60045 USA

 

RL-0000

Sodium Chloride

Sodium Chloride

SODIUM CHLORIDE INJECTION, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:0409-1918
Route of Administration INTRAVENOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE 9 mg

Inactive Ingredients

Ingredient Name Strength
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 2 in 1 CARTRIDGE
2 3 in 1 CARTRIDGE
3 5 in 1 CARTRIDGE
4 NDC:0409-1918-35 25 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-09-13


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.