Etomidate Injection, Solution
Product Images NDC 65219-445

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Etomidate (NDC 65219-445). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structural Formula (Eto06 0000 01)

Chemical structure of Etomidate, depicting the molecular arrangement including a central carbon linked to an imidazole ring, ester functional group, and phenyl ring consistent with the etomidate molecule.*

FDA Label Image

Fresenius Kabi Logo (Eto06 0000 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY –Etomidate Injection, USP Single-Dose Vial Label)

Label for Etomidate Injection, USP 20 mg/10 mL (2 mg/mL) intravenous solution, single-dose vial. The label includes dosage strength, usage instructions for intravenous use only, storage conditions, and manufacturer information for Fresenius Kabi USA, LLC. Additional details include propylene glycol content and water for injection.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY –Etomidate Injection, USP Single-Dose Carton)

Etomidate Injection, USP 2 mg/mL (20 mg/10 mL) intravenous solution packaging label for single-dose vials. The label indicates it is for intravenous use only and contains 10 vials per package. The product is labeled by Fresenius Kabi USA, LLC and includes manufacturing details, storage instructions, and a barcode. It also lists inactive ingredients such as propylene glycol and water for injection.*

* 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.