Auvi-q Injection, Solution
Product Images NDC 51662-1663

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Auvi-q (NDC 51662-1663). 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

Structure (51662 1661 Structure)

Chemical structure diagram of the active ingredient in AUVI-Q injection solution, showing a catechol ring with hydroxyl groups, a side chain with an alcohol group, and an amine functional group, consistent with epinephrine's molecular structure.*

FDA Label Image

How Supplied (51662 1661 How Supplied)

A table listing package configurations, strengths, and corresponding NDC numbers for AUVI-Q injection. It includes single and double autoinjector packages at strengths 0.3 mg, 0.15 mg, and 0.1 mg, each with unique NDC codes.*

FDA Label Image

Serialized Label (51662 1663 1)

A white label with black text showing GS1 barcoding data including (01) GTIN, (17) expiration date, (21) serial number, and (10) lot number. The label instructs to see the manufacturer's insert and states distribution by HF Acquisitions Co., LLC in Mukilteo, WA 98275. There is a vertical 2D barcode on the right side. The label is related to the AUVI-Q injection, solution product.*

FDA Label Image

Serialized Label (51662 1663 2)

A white pharmaceutical label for AUVI-Q injection, solution .3 mg/.3 mL distributed by HF Acquisitions Co., LLC, Mukilteo, WA 98275. The label includes various barcode digits and a vertical 2D barcode on the right side, with instructions to see the manufacturer's insert.*

* 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.