Product Images Esmolol Hydrochloride

This is a single-dose container of Esmolol HCI in Sodium Chloride Injection, with a concentration of 2,500mg per 250 mL (10mg/mL). The solution is intended for single intravenous use only, is iso-osmotic and free of preservatives. Each mL contains 10mg of Esmolol HCI USP, 5.9mg of sodium chloride USP in water for injection USP, buffered with 2.8mg sodium acetate trinydrate USP and 0.546mg glacial acetic acid USP. It is sterile, non-pyrogenic, and has a pH of 5.0 (4.5 to 5.5). It is not safe to use if the overwrap has been previously opened or damaged. After removing the overwrap, check for leaks by squeezing the container firmly. The solution must be clear and colorless to light yellow in color. Unused portions of the solution must be discarded. It must not be used in series connections, and must be stored at 25°C (77°F) with excursions permitted to 15° to 30°C (59° to 86°F).*

This is a single-dose container that contains 2,500 mg of Esmolol HCI in 250 mL of Sodium Chloride Injection with a concentration of 10 mg/mL. The solution is iso-osmotic and does not have any preservatives. It is for single intravenous use only and contains acetate trihydrate USP and 0.546 mq glacial acetic acid USP. It has a pH between 4.5 and 5.5, adjusted with sodium hydroxide and/or hydrochloric acid. It should be stored at a temperature between 15-30°C (59-86°F) and protected from light. The container was manufactured by AuroMedics Pharma LLC in E. Windsor, NJ with the product code T/DRUGS/012013AVP.*

This appears to be a label for a medication called Esmolol HCI, provided with a prescription (Rx) and an NDC number for identification. It is an isotonic solution of the medication in sodium chloride and is intended for intravenous (IV) use. The label includes space for the patient name, date, time of infusion, and the name of the person who started the infusion. Finally, the label instructs to apply it to the IV bag.*

This is a 100 mL single-dose container of Esmolol HCI in Sodium Chloride Injection with 2,000 mg per 100 mL. It is a double-strength intravenous medication for single use only with no preservative added. It contains 20 mg esmolol hydrochloride USP, 4.1 mg sodium chloride USP, and other USP ingredients. The usual dosage is listed on the package. It is manufactured in India by AuroMedics Pharma LLC, and it is Rx only. Check for leaks before use, and discard if the solution is not clear or if the container is leaking. Store at room temperature and avoid excessive heat and freezing.*

This is a description of a single dose container of Esmolol HCI in Sodium Chloride Injection, containing 2,000 mg per 100 mL. The product must not be used in series connections, and additives should not be introduced. The product must be stored at a controlled room temperature, with protection from freezing and excessive heat. The recommended dosage should be consulted on the package insert, and it is important to check for leaks before using the product. The product is sterile and non-pyrogenic. The container should not be removed from the overwrap until ready to use, and if the overwrap has been previously opened or damaged, the product should not be used. The pH value of the solution is 5.0.*

This is a 100mL Single-Dose container of Esmolol HCI Rx which contains 2000 mg per 100 mL in Sodium Chloride Injection. It is meant for single intravenous use only and is iso-osmotic with no preservative added. Each mL contains 20mg esmolol hydrochloride USP, 4.1mg sodium chloride USP in water for injection USP. It is buffered with sodium acetate trihydrate USP and acetic acid USP. The pH is adjusted with sodium hydroxide and/or hydrochloric acid with pH 5.0 (4.5 to 5.5). It is sterile and nonpyrogenic with specific storage requirements. Usual Dosage: See packaging insert. However, it should not be used in series connections, and additives should not be introduced.*

This is a prescription drug with the NDC 55150-421-01 code. The drug is Esmolol HCI which is a double strength solution in Sodium Chloride Injection. It is an Iso-Osmotic solution that contains Esmolol Hydrochloride in Sodium Chloride. The other details on the label are related to the administration of the drug, such as the name of the patient, the start time of infusion, the person who started it, and a P1428320 identification code.*