Etomidate Injection, Solution
Product Images NDC 51662-1634

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Etomidate Injection, Solution (NDC 51662-1634). 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.

Product Images & Figures Index

FDA Label Image

Serialized Label (51662 1634 1 Serialized Label)

Serialized Label (51662 1634 1 Serialized Label)
Detail of a label from ETOMIDATE injection, solution showing a barcode and numeric identifiers, with text instructing to see manufacturer's package insert. It notes distribution by HF Acquisition Co, LLC in Mukilteo, WA, and includes 'RX ONLY' indicating prescription use.*
FDA Label Image

Structure (51662 1634 1 Structure)

Structure (51662 1634 1 Structure)
Chemical structure of etomidate, shown with its molecular components and rings. The image also includes a brief textual note stating that Etomidate USP is a white or almost white powder.*
FDA Label Image

Mfg Container Label (Mfg Container Label)

Mfg Container Label (Mfg Container Label)
Label for Etomidate Injection, USP 20 mg per 10 mL (2 mg/mL) solution in a single-dose vial for intravenous use. The label states it is sterile and nonpyrogenic, contains Etomidate USP 2 mg per mL, and includes propylene glycol 35% w/v. Storage instructions and manufacturer information for Euga US LLC, Milford, Indiana, are also present, along with an NDC barcode 55150-221-10.*

* 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.