Dual Port Bag (Image 01)
Esmolol Hydrochloride In Water Injection
Product Images NDC 44567-811
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Esmolol Hydrochloride In Water (NDC 44567-811). 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.
Structural Formula (Image 02)
Esmolol 2000 mg/100 mL Overwrap (Image 03)
The text is a product label of Esmolol Hydrochloride in Water for Injection. It comes in a 100 mL container with tear notch to open. It must be stored within 20° to 25°C and protected from freezing. The container closure is free from natural rubber latex. The label warns the user not to introduce additives and not to use in series connections.*
Esmolol Hydrochloride 2500 mg/250 mL Overwrap (Image 04)
This is a prescription medication called Esmolol Hydrochloride that is administered intravenously. It is sterile, non-pyrogenic, and doesn't have preservatives. Each mL contains Esmolol Hydrochloride, Ethanol, Propylene Glycol, and water that has been buffered with Sodium Acetate Trihydrate and Glacial Acetic Acid. The pH is adjusted with Sodium Hydroxide. The usual dosage should be determined by the physician. The medication should be used with caution since sterility can be impaired if leaks are found, and it should only be used if it is clear and colorless, with no other additives. The medication should not be used in a series of connections. The storage temperature range permitted is from 15°C to 30°C (59°F to 86°F), and it should be kept in the overwrap to maintain sterility.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
