Penicillin G Potassium Injection, Solution
Product Images NDC 0338-1025

Baxter Penicillin G Potassium Injection, USP is a medication used for intravenous use as directed by a physician. It is available in a 50 mL bottle that contains Penicillin G Potassium, USP equivalent to 1,000,000 units Penicillin G with approximately 2 g Dextrose Hydrous, USP added for viscosity and 100 mg Sodium Citrate, USP added as a buffer. The pH is adjusted with hydrochloric acid and may have been adjusted with sodium hydroxide. The solution has a pH of 6.5 (5.5 to 8.0). The solution needs to be stored at or below -20°C/-4°F and should be thawed at room temperature or under refrigeration (5°C/41°F). The thawed solution is stable for 14 days under refrigeration or 24 hours at room temperature. This medication must not be used in series connections and should be checked for minute leaks and solution clarity before use. Adding supplementary medication is not recommended. Baxter and Galaxy are registered trademarks of Baxter International Inc.*

This text provides instructions for handling and thawing Baxter Penicillin G Potassium Injection, which comes in single-dose containers. It cautions against forcing the thawing process and recommends handling frozen containers with care. The product should be stored at a temperature of -20°C/-4°F and should not be refrozen once thawed. The thawed solution can be stored for up to 14 days under refrigeration or for 24 hours at room temperature. The product is identified by the NDC code 0338102141 and the trademarked names Bartr and Galay.*

This appears to be a description of a sterile medical product called GALAXY Cartainer. It contains Penicillin and Polasiu, among other things, and is meant to be injected intravenously. The text contains dosage information and warnings not to use the product if contaminated or if there are signs of damage to the packaging. The product is only available with a prescription.*

This is a description of Baxter's Penicillin G Potassium Injection, which is a medication used for intravenous treatment as directed by a physician. Each 50mL contains Penicillin G Potassium, USP equivalent to 2,000,000 units Penicillin G, dextrose, hydrous, USP, and sodium citrate, USP added to adjust osmolarity and buffer respectively. The medication is cautioned for not adding supplementary medication and not used in serious conditions. The solution is stored in a freezer below -20°C/-4%F and thawed at room temperature or under refrigeration. This medication is produced by Baxter Healthcare Corporation, and it appears to be registered under Baxter and Galaxy trademarks.*

This appears to be descriptions of two different products labeled as GALAXY Cartainer Sterle Nanpyragenic and GALAXY Cortainer Strie Nonpyrogenic respectively. The first one includes 5D exchange containing Penillin and Potassium, and Hyirus and SP additives. The pH level was adjusted using yoclonc acid and Sodium, and it is not recommended to add supplementary medication to it. It should be used with caution since it may cause damage to the veins if not used properly. The second one appears to contain Eniclin G Potassium with some additives such as Hyorous and Sodu Ciat. The pH level was also adjusted, and it should not be used in situations where there is a risk of infection. It is not advisable to add any supplementary medication to it as it may impair its efficiency. It should be used only under medical prescription.*

This is a description of Baxter's Penicillin G Potassium Injection, USP which comes in a 50mL GALAXY container with an NDC number of 0338-1025-41. Each 50 mL of the injection contains 3,000,000 units of Penicillin G Potassium, and has approximately 350mg of Dextrose Hydrous, USP added for osmolality adjustment and 300mg of Sodium Citrate, USP (0.3g as a buffer). The solution is adjusted with hydrochloric acid or sodium hydroxide to pH 6.5 (5.5 to 8.0). The injection is to be administered intravenously, dosage as directed by the physician. However, no additional medication should be added, and it should not be used in series connections. The injection should be checked for minute leaks and solution clarity. The product should be stored below -20°C/-4°F, and thawed at room temperature of 26°C/77°F, or under refrigeration (5°C/41°F). The solution is stable for 14 days if refrigerated or 24 hours if kept at room temperature. Not to be frozen.*

This is a set of instructions for handling and thawing a frozen medical product called Penicillin G Potassium Injection, USP. It is recommended to thaw the product under refrigeration or at room temperature, but not by immersion in water baths or microwave irradiation. The product container may be fragile when frozen, so it should be handled with care. Once thawed, the solution should not be refrozen and is only stable for a limited time under refrigeration or at room temperature. The text also includes information about the manufacturer and product codes.*