Country: মার্কিন যুক্তরাষ্ট্র
ভাষা: ইংরেজি
সূত্র: NLM (National Library of Medicine)
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698)
Cardinal Health
SODIUM CHLORIDE
SODIUM CHLORIDE 9 mg in 1 mL
INTRAVENOUS
PRESCRIPTION DRUG
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.
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
New Drug Application
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 সম্পূর্ণ নথি পড়ুন