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Appropriate sterile vehicles for solutions or suspensions for parenteral injection other than WFI may include which of the following?Select all that apply A. Ringer's Injection, USP B. Bacteriostatic Sodium Chloride Injection, USP C. Sodium Chloride Injection, USP D. Benzyl Alcohol

Question

Appropriate sterile vehicles for solutions or suspensions for parenteral injection other than WFI may include which of the following?Select all that apply A. Ringer's Injection, USP B. Bacteriostatic Sodium Chloride Injection, USP C. Sodium Chloride Injection, USP D. Benzyl Alcohol

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Solution

The appropriate sterile vehicles for solutions or suspensions for parenteral injection other than Water for Injection (WFI) may include:

A. Ringer's Injection, USP: This is a sterile solution used for intravenous administration. It contains multiple electrolytes in a specific concentration, and it's often used as a fluid and electrolyte replenisher.

B. Bacteriostatic Sodium Chloride Injection, USP: This is a sterile, nonpyrogenic, isotonic solution of sodium chloride. It contains an antimicrobial agent that helps to prevent the growth of bacteria, making it suitable for multiple-dose vial usage.

C. Sodium Chloride Injection, USP: This is a sterile solution of sodium chloride in water for injection. It's used as a vehicle for the administration of a drug or as a diluent and dispersing agent for a suspension.

D. Benzyl Alcohol: This is not typically used as a vehicle for parenteral injection. It's often used as a preservative in some injection preparations. However, it's not suitable for use in neonates due to the risk of toxicity.

So, the correct answers would be A, B, and C.

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Similar Questions

Which of the following is not a requirement for the packaging of sterile injectable products? A. Single dose products must be packaged in vials or ampules that contain less than 30 ml. B. A single dose container must be hermetic but once it has been opened it cannot be resealed with assurance that sterility has been maintained. C. A multi-dose container must be hermetic, but due to the packaging, the sterility of the contents is maintained to allow withdrawal of successive doses. D. The material of the container and its closure must not interact with the drug preparation in a way that alters the strength or efficacy of the product.

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