Etomidate Injection
Product Images NDC 51662-1485

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Etomidate (NDC 51662-1485). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Pplied (How Supplied)

A data table listing Etomidate 2 mg/mL injection available in two container sizes: 10 mL and 20 mL. Each comes in a carton containing 10 vials. The table provides corresponding NDC numbers for each size.*

FDA Label Image

Serialized Labeling (Seerialized Vial Labeling)

Vial of Etomidate Injection USP 2 mg/mL for intravenous use, labeled with NDC 0143-9506-01. The label indicates the solution strength as 20 mg/10 mL (2 mg/mL) and features the HF Acquisition Co LLC, DBA HealthFirst logo. A secondary label displays a barcode and distribution information for HF Acquisition Co LLC, Mukilteo, WA.*

FDA Label Image

Structure (Structure)

Chemical structure of Etomidate, showing its molecular arrangement with a 2-methylimidazole ring, an ester functional group, and a phenyl group attached to a central carbon.*

FDA Label Image

Vial Label (Vial Label)

Label for Etomidate Injection, USP 20 mg/10 mL (2 mg/mL) single-dose vial for intravenous use. The label indicates the active ingredient concentration and propylene glycol 35% v/v content. It is sterile and nonpyrogenic. Storage instructions specify 20°C to 25°C, with manufacturing by Hikma Farmacêutica in Portugal and distribution by West-Ward in Eatontown, NJ. The label includes a barcode and space for lot and expiration dates.*

* 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.