Esmolol Hydrochloride Injection, Solution
Product Images NDC 25021-309

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Esmolol Hydrochloride (NDC 25021-309). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Figure 2 (Esm01 0005 01)

An instructional diagram showing a dual-port intravenous bag with labels indicating a delivery port and a medication port for withdrawing the initial bolus only. This illustration is related to the intravenous administration of esmolol hydrochloride injection solution.*

FDA Label Image

Structural Formula (Esm01 0005 02)

Chemical structure diagram of esmolol hydrochloride, showing its molecular formula with benzene ring and associated functional groups as presented.*

FDA Label Image

Package Label – Principal Display Panel – Bag Label (Esm01 0005 03)

Label for Esmolol Hydrochloride in Sodium Chloride Injection, 10 mg/mL concentration, with a total of 2,500 mg in 250 mL. The label indicates single-dose use, intravenous administration only, and includes storage instructions. It is manufactured for Sagent Pharmaceuticals and lists inactive ingredients and handling warnings.*

FDA Label Image

Package Label – Principal Display Panel – Bag Label (Esm01 0005 04)

Label for Esmolol Hydrochloride in Sodium Chloride Injection, 20 mg/mL (2,000 mg per 100 mL) intravenous solution by Sagent Pharmaceuticals. The single-dose vial contains esmolol hydrochloride and sodium chloride in a buffered solution. Storage instructions and usage warnings are included, along with the manufacturer's information and barcode.*

* 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.