Esmolol Hydrochloride Injection
Product Images NDC 44567-450

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Esmolol Hydrochloride (NDC 44567-450). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wg Critical Care, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Esmolol HCl In Sodium Chloride Injection Bag 2500 mg/250 mL (Image 01)

Esmolol HCl In Sodium Chloride Injection Bag 2500 mg/250 mL (Image 01)
This is a description of a medication with National Drug Code (NDC) 4456745001, containing a solution of 500mg Esmolol Hydrochloride per 250 mL of sodium chloride injectable solution intended for single intravenous use only. Each milliliter contains 10mg Esmolol Hydrochloride, 5.9mg Sodium Chloride, buffered with 2.8mg Sodium Acetate Trihydrate and 0.546mg Glacial Acetic Acid. It is a sterile, non-pyrogenic solution that is isotonic with no preservative added. The drug should not be used in series connections and should not have additives added to it. It also comes with several cautionary notes, such as checking for leaks in the container, discarding unused portions, not being used if there are leaks and being stored at 25°C with excursions permitted at15°C to 30°C. The medication has been made in Switzerland.*
FDA Label Image

Esmolol HCl In Sodium Chloride Injection 2000 mg/100 mL Bag (Image 02)

Esmolol HCl In Sodium Chloride Injection 2000 mg/100 mL Bag (Image 02)
Esmolol Hydrochloride is a medication used for intravenous use only. This drug is a double strength solution that contains 20mg of Esmolol Hydrochloride USP, 4.1 mg of Sodium Chloride USP, buffered with 2.8 mg of Sodium Acetate Trihydrate USP and 0.546 mg of Glagal Acetic Acd USP. It has a pH of 5.0 and is sterile and non-pyrogenic. This solution is prescribed to patients according to the package insert. To check for leaks, the container must be squeezed firmly, and if any leaks are found, it should be discarded. The solution must not have any additives, and unused portions should be discarded after use. It must be stored at 25°C (77°F), and protection from freezing and excessive heat must be ensured. This product has been produced in Switzerland.*
FDA Label Image

Iv Bag Image (Image 03)

Iv Bag Image (Image 03)
This text is describing the medication port for withdrawing an initial bolus, and a delivery port.*
FDA Label Image

Esmolol Hydrochloride Structural Formula (Image 04)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.