Sodium Chloride 0.9% For Injection Single Dose Vials 2 mL x 25/Pack (RX)

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Sodium Chloride 0.9% For Injection 2mL, 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 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.
Manufacturer: APP Pharmaceuticals
Application: Diluent
Container Type: Single Dose Vial
Generic Drug Name: Sodium Chloride, Preservative Free
NDC Number: 63323-0186-02
Storage Requirements: USP Controlled Room Temperature
Strength: 0.9%
Type: Intramuscular, Intravenous, or Subcutaneous
Volume: 2 mL
Sodium Chloride 0.9% For Injection 2mL, 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 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.
Manufacturer: APP Pharmaceuticals
Application: Diluent
Container Type: Single Dose Vial
Generic Drug Name: Sodium Chloride, Preservative Free
NDC Number: 63323-0186-02
Storage Requirements: USP Controlled Room Temperature
Strength: 0.9%
Type: Intramuscular, Intravenous, or Subcutaneous
Volume: 2 mL
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