Product Images Potassium Chloride In Dextrose And Sodium Chloride

This is a description of a medication in liquid form for intravenous use. It contains potassium chloride, sodium chloride, and dextrose in water for injection, with electrolytes per 1000 mL being 20 mEqg potassium, 77 mEg sodium, and 97 mEq chloride. The package insert should be consulted for the usual dosage, and the container should be discarded if unused. The overwrap is a moisture barrier, and the medication should be used immediately once removed from this barrier. The container closure is not made with natural rubber latex, and it is non-PVC, non-DEHP, and sterile. The medication is manufactured in Norway by Fresenius KABI for distribution in the US.*

This is a product description for a 0.45% Sodium Chloride Injection, USP in 500 mL x 20 quantities with NDC code 65219-150-75. It should be stored at a controlled room temperature of 20° to 25°C (68° to 77°F) and protected from freezing and excessive heat. The product is manufactured for Fresenius in Lake Zurich, IL 60047 and made in Norway. The expiration date is listed as MM-YYYY and the product LOT is 0000000.*

This is a sterile intravenous solution containing potassium chloride, sodium chloride, and dextrose in water for injection. Each 100 mL contains 74.5 mg of potassium chloride, 450 mg of sodium chloride, and 5 g of dextrose hydrous. This solution is intended for the base supplementation of fluids, electrolytes, and calories. The electrolyte content per 1000 mL of the solution are: Potassium 10 mEq, Sodium 77 mEq, Chloride 87 mEq. It is a single-dose container, and unused portions should be discarded. This solution should be stored in a controlled room temperature of 20° to 25°C, and should be protected from freezing. Additives may be incompatible; therefore, consult with a pharmacist in case an additive is introduced into the solution. The overwrap is a moisture barrier, and it should be removed immediately before use. The container closure is latex-free. The manufacturer is Fresenius Kabi, and the solution is made in Norway.*

This is a description of a medication with the National Drug Code (NDC) 65219-142-10. The medication is Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection USP, and it comes in 1000 mL x 10 bottles. The medication should be stored between 20 to 25°C (68 to 77°F) in a controlled room temperature, and should be protected from freezing and excessive heat. This medication is manufactured in Norway and the LOT number is 0000000.*

This is a description of a single-dose container of POTASSIUM CHLORIDE in 5% Dextrose and 0.45% Sodium Chloride Injection, USP. Each container of 1000 mL contains 20 mEq POTASSIUM. It is meant for intravenous use and should be stored at 20° to 25°C (68° to 77°F) to avoid excessive heat. The electrolytes per 1000 mL (not including ions for pH adjustment) are Potassium 20 mEq, Sodium 77 mEg and Chloride 97 mEg.*

This is a description of a medication with the National Drug Code 65219-144-10. The medication is a solution containing Potassium Chloride along with 5% Dextrose and 0.45% Sodium Chloride Injection in a 1000 mL bag. The solution is manufactured in Norway and packaged in Lake Zurich, IL. The medication must be stored at 20° to 25°C, and protected from freezing and excessive heat. The rest of the text is not included, as it contains unclear characters and symbols.*

This is a description of an intravenous electrolyte solution containing potassium chloride, sodium chloride, and dextrose, used for replenishing the body's electrolytes. It is recommended to consult a pharmacist when introducing additives, and the product should be discarded if the seal is broken. The overwrap serves as a moisture barrier, and it is advised to use the product immediately once removed from the overwrap. The solution should be stored at controlled room temperature, and protected from freezing. The container closure is not made with natural rubber latex, and the product is made in Norway by Fresenius Kabi.*

This is a description of a medication with the NDC code 65219-146-10. The medication contains a mixture of Potassium Chloride, 5% Dextrose, and 0.45% Sodium Chloride Injection. It is available in 1000 mL x 10 packs and is manufactured by a company based in Lake Zurich, IL 60047. It should be stored at 20° to 25°C (68° to 77°F) to protect from freezing and excessive heat. However, it states that it is made in Norway. The other text such as YYMMDD, 17, and 01-82-16-018, do not provide any relevant information.*

This is a description of a medication, containing potassium chloride, which is used for intravenous use. The medication contains 40 mEq of potassium, 77 mEq of sodium, and 117 mEq of Chloride per 1000 mL. The medication is provided in a single-use container and has to be used immediately once the cover is removed. There are specific instructions provided to handle the introduction of additives to the medication. The medication needs to be stored at 20° to 25°C (68° to 77°F).*

This is a description of a medication with National drug code (NDC) 65219-148-10 and lot number 244810. The medication is Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP in a 1000 mL package which includes 10 individual packages. The medication should be stored at room temperature (20°C to 25°C) and protected from freezing and excessive heat. The medication is manufactured in Norway and distributed by a company located in Lake Zurich, IL. The expiration date is not specific but marked as MM-YYYY, and the lot number is 0000000 with a quantity of 10.*