SODIUM CHLORIDE- sodium chloride injection, solution

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Aktīvā sastāvdaļa:

SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698)

Pieejams no:

Cardinal Health

SNN (starptautisko nepatentēto nosaukumu):

SODIUM CHLORIDE

Kompozīcija:

SODIUM CHLORIDE 9 mg in 1 mL

Ievadīšanas:

INTRAVENOUS

Receptes veids:

PRESCRIPTION DRUG

Ārstēšanas norādes:

This parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.

Produktu pārskats:

0.9% Sodium Chloride Injection, USP is supplied in the following: NDC No. Container Size 55154-0103-8 Overbagged with 1 vial per bag Fliptop Plastic Vial 20 mL Store at controlled room temperature 20 to 25°C (68 to 77°F) [See USP Controlled Room Temperature.] Instructions for Use of the Syringe Systems Instructions for using the Carpuject Syringe are available with the reusable Carpuject Holder, List 2049-02. Revised:9/2015  EN-4029 Hospira, Inc., Lake Forest, IL 60045 USA                                                                                 

Autorizācija statuss:

New Drug Application

Produkta apraksts

SODIUM CHLORIDE- SODIUM CHLORIDE INJECTION, SOLUTION
CARDINAL HEALTH
----------
0.9% SODIUM CHLORIDE
Injection, USP
CARPUJECT™ WITH LUER LOCK
FLIPTOP PLASTIC VIAL
LIFESHIELD™ FLIPTOP PLASTIC VIAL
Rx only
DESCRIPTION
This preparation is designed solely for parenteral use only after
addition of drugs that require dilution
or must be dissolved in an aqueous vehicle prior to injection.
0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic,
isotonic solution of sodium chloride
and water for injection. Each mL contains sodium chloride 9 mg. It
contains no bacteriostat,
antimicrobial agent or added buffer and is supplied only in
single-dose containers to dilute or dissolve
drugs for injection. 0.308 mOsmol/mL (calc.). 0.9% Sodium Chloride
Injection, USP contains no
preservatives. The solution may contain hydrochloric acid and/or
sodium hydroxide for pH adjustment.
pH 5.3 (4.5 to 7.0).
Sodium Chloride, USP is chemically designated NaCl, a white
crystalline compound freely soluble in
water.
The glass container is a Type I borosilicate glass and meets the
requirements of the powdered glass
test according to the USP standards.
The semi-rigid vial is fabricated from a specially formulated
polyolefin. It is a copolymer of ethylene
and propylene. The safety of the plastic has been confirmed by tests
in animals according to USP
biological standards for plastic containers. The container requires no
vapor barrier to maintain the
proper drug concentration.
CLINICAL PHARMACOLOGY
Sodium chloride in water dissociates to provide sodium (Na ) and
chloride (Cl‾) ions. These ions are
normal constituents of the body fluids (principally extracellular) and
are essential for maintaining
electrolyte balance.
The distribution and excretion of sodium (Na ) and chloride (Cl‾)
are largely under the control of the
kidney which maintains a balance between intake and output.
_PRESERVATIVE-FREE_
_ _
+
+
The small volume of fluid and amount of sodium chloride provided by
0.9% Sodium Chloride Injection,
USP when used only as an isotoni