| Application: | Internal Medicine |
|---|---|
| Usage Mode: | Injection |
| Suitable for: | Children, Adult |
| State: | Liquid |
| Type: | Inorganic Chemicals |
| Pharmaceutical Technology: | Chemical Synthesis |
| Customization: |
|---|
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Audited Supplier Sodium Chloride Injection, USP is indicated as a source of water and electrolytes.
0.9% Sodium Chloride (sodium chloride (sodium chloride injection) injection) Injection, USP is also indicated for use as a priming solution in hemodialysis procedures.
As directed by a physician. Dosage is dependent upon the age, weight and clinical condition of the patient as well as laboratory determinations.
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. Do not administer unless solution is clear and seal is intact.
All injections in AVIVA plastic containers are intended for intravenous administration using sterile equipment.
Additives may be incompatible. Complete information is not available. Those additives known to be incompatible should not be used.
Consult with pharmacist, if available. If, in the informed judgment of the physician, it is deemed advisable to introduce additives, use aseptic technique. Mix thoroughly when additives have been introduced. Do not store solutions containing additives.
Sodium Chloride Injection, USP should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
In patients with diminished renal function, administration of Sodium Chloride (sodium chloride (sodium chloride injection) injection) Injection, USP may result in sodium retention.
Character:Colorless clear liquid; taste brackish.
Storage and sealed storage.
Package: 10 ml: 90 mg
100ml: 0.9g
250 ml: 2.25g
500ml : 4.5g
1000ml / 9g
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Audited Supplier 
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