Sodium Chloride (Sodium Chloride)

Trade Name : SODIUM CHLORIDE

Liebel-Flarsheim Company LLC

INJECTION

Strength 0.9 mg/mL

SODIUM CHLORIDE Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]

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Product information is meant for

Wholesalers Suppliers Exporters Doctors MOH Tender Supplies Hospitals Brand CROs Comparator Supplies Generic Cooperate Sourcing Individual Patients Indian Institutional Buyers

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Sodium Chloride (Sodium Chloride) which is also known as SODIUM CHLORIDE and Manufactured by Liebel-Flarsheim Company LLC. It is available in strength of 0.9 mg/mL per ml. Read more

Sodium Chloride (Sodium Chloride) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials. Click to know price. Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

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No data

For use in flushing compatible contrast agents throughu00a0Liebel-Flarsheimu00a0intravenous administration sets into indwelling intravascular access devices ()

No data

For single patient use only. ()
Determine the volume of flush based on the imaging procedure, location of the vascular access device, length of tubing between power injector and vascular access device, and the contrast agent package insert. ()
Individualize the volume of flush based on body weight, fluid status and concomitant medical conditions. ()
Typical flush volumes for adults are 10 to 25 mL per injection at rates not to exceed 10 mL/sec. ()
May be used for additional infusion to maintain the patency of vascular access at a typical infusion rate of 0.5 to 1 mL per minute. ()
Do not use if packaging is damaged, wet, or not intact, if syringe or its tip cap shows signs of damage, leakage or displacement. Do not use if solution is hazy, cloudy, discolored, or contains particulate matter. ()
Use aseptic technique. ()
Expel residual air from the syringe and tubing prior to connection with the patientu2019s vascular access. ()n

Sodium Chloride Injection USP (0.9%)

Supplied as a clear, colorless, odorless, sterile solution of Sodium Chloride 0.9% for intravenous administration ()
Supplied in 125 mL prefilled syringes ()

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None ()

No data

Remove all air from the syringe and associated tubing prior to injection. ()
May cause fluid overload in patients with congestive heart failure, severe renal insufficiency, and in clinical states with edema, sodium retention, or hypernatremia. ()
Establish intravascular catheter patency prior to administration. ()n

Reported adverse reactions include:
To report SUSPECTED ADVERSE REACTIONS, contact Liebel-Flarsheim Company LLC at 1-855-266-5037 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.u00a0u00a0

Adverse reactions due to solution or administration technique may include: air embolism with stroke, chest pain, and dyspnea, arrhythmia, hypotension, myocardial infarction, sepsis, febrile response, local tenderness, infection at the site of injection, venous thrombosis or phlebitis extending from injection site, extravasation, fluid overload and hypervolemia. ()

No data

Pregnancy: It is not known whether Sodium Chloride Injection USP 0.9% can cause fetal harm. ()
Pediatrics: Safety and effectiveness have not been established in pediatric patients. ()
Geriatrics: Dosing for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. ()n

Use of Sodium Chloride Injection USP 0.9% may pose a threat of overdose marked by electrolyte disturbance and/or fluid overload, particularly in pediatric patients and patients with compromised renal or cardiac function. In the event of overdosage, discontinue the infusion, reevaluate the patient and institute appropriate corrective action.

Sodium Chloride Injection USP 0.9% is a formulation of sodium chloride in Water for Intravascular Injection. No preservative, antimicrobial agent or buffer is added. Sodium Chloride Injection USP 0.9% is provided as a sterile, nonpyrogenic, clear, colorless, odorless solution.n n n n Each mL of Sodium Chloride Injection USP 0.9% contains 9 mg of sodium chloride. The pH is 4.5 to 7.0. The osmolarity is 308 mOsm/L (calc.). u00a0n Sodium Chloride Injection USP 0.9% is provided in a 125 mL syringe with a 125 mL fill.u00a0 The syringes are for single patient use and are disposable and not meant for reuse. n

Sodium Chloride Injection USP 0.9% has an osmotic pressure similar to plasma.

Sodium Chloride Injection USP 0.9% is a clear, colorless, odorless solution containing 9 mg/mL of sodium chloride. Sodium Chloride Injection USP 0.9% is supplied in 125 mL prefilled syringes containing 125 mL of solution. Each syringe is sealed with rubber closures and the contents are sterile. The 125 mL syringe is supplied with a luer locknut adapter which is cleared for manufacture and distribution as a device under 510(K) number 862653. The syringes are contained in shipping cartons with the following configurations:
RFID-Tagged Syringe Description
This information is for Ultraject syringes containing Sodium Chloride Injection USP 0.9% that has been labeled with a Radio Frequency Identification (RFID) tag.u00a0 When used with an RFID-enabled Optivantage Injector, this tag allows for the exchange of product information such as lot number, expiration, concentration, and identification of the syringe as being unused prior to use and used after product administration.u00a0 Patient information is not utilized in any form with this RFID technology. Sodium Chloride Injection USP 0.9% product quality is not impacted with the use of this RFID tag. Sodium Chloride Injection USP 0.9% RFID syringes require no special handling and should be stored at the conditions listed for the drug product.
RFID-Tagged Syringe Directions for Use
For the RFID technology to function, the syringe must be used with an Optivantage Injector with RFID technology. Function of the RFID technology is not dependent on syringe orientation as it is placed in the injector. Instructions for use of the injector are provided on the injector interface screens and operatoru2019s manual.
If the RFID tag is damaged or otherwise non-functional, the injector will notify the user.u00a0 Should this occur, the Sodium Chloride Injection USP 0.9% syringe with the non-functional RFID tag may still be used but no data will be transferred to the injector.
Regarding interference with medical devices, the RFID tag and injector system meet the IEC 60601-1-2 requirements for emission and immunity standards for medical devices.u00a0 Follow all manufacturersu2019 guidelines and do not operate any part of the Optivantage Injector System and RFID-tagged syringes within 6 inches (15 cm) of a pacemaker and/or defibrillator.
Storage
Store Sodium Chloride Injection USP 0.9% syringes and RFID-tagged syringes at 25u00b0C (77u00b0F); excursions permitted to 15u00b0 to 30u00b0C (59u00b0 to 86u00b0F) n
PROTECT FROM FREEZING
Manufactured by:Liebel-Flarsheim Company LLCRaleigh, NC 27616
Made in USA
GBTu00a011880919u00a0
Issued: 9/19
Guerbet

For Intravascular Use
Sterile Solution
NDC 0019-1188-81
125 mL
Sodium Chloride Injection USP 0.9%
MEDICATION AND FLUID PATHWAY ARE STERILE.OUTSIDE OF SYRINGE IS NOT STERILE.
SINGLE DOSE UNIT, DISCARD UNUSED PORTION.n- EXPEL AIR BEFORE USE.n- PROTECT FROM FREEZING.
Rx only
Store at 25u00b0C (77u00b0F); excursions permitted to 15u00b0 to 30u00b0C (59u00b0 to 86u00b0F) [see USP Controlled Room Temperature].
Each mL contains 9 mg sodium chloride.n- Dosage: See package insert.n- Discard if syringe seal is broken or leakage is observed.
Manufactured by:Liebel-Flarsheim Company LLCRaleigh, NC 27616Made in USA
Guerbet
12070916

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Sodium Chloride (Sodium Chloride)

Trade Name : SODIUM CHLORIDE

INJECTION

Delivery Process

Product information is meant for

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

Packaging and Delivery

About GNH

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Sodium Chloride (Sodium Chloride)

Trade Name : SODIUM CHLORIDE

INJECTION

Delivery Process

Product information is meant for

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

Packaging and Delivery

About GNH

Similar Products

Desogestrel And Ethinyl Estradiol (Emoquette)

Diphenoxylate Hydrochloride And Atropine Sulfate (Diphenoxylate Hydrochloride And Atropine Sulfate)

Fluoxetine Hydrochloride (Fluoxetine)

Metoprolol Succinate (Metoprolol Succinate)

Losartan Potassium (Losartan Potassium)

Browse Our Services And Processes

Disclaimer

Browse from other international pharmaceuticals

General

US NDC

Canadian DIN

Swiss Drugs

NZ Drugs

FAQ

Can’t find what you’re looking for?

COMPANY

SERVICES

QUICK LINKS

CONTACT US

Can’t find what
you’re looking for?