Auvi-q Injection, Solution
Product Images NDC 51662-1661

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Auvi-q (NDC 51662-1661). 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 showing the molecular arrangement of the active ingredient in AUVI-Q injection, solution 0.1 mg/0.1 mL.*

FDA Label Image

How Supplied (51662 1661 How Supplied)

A data table showing package configurations, strengths, and National Drug Codes (NDCs) for AUVI-Q autoinjectors. It lists configurations of 1 or 2 autoinjectors with strengths of 0.3 mg, 0.15 mg, and 0.1 mg, each associated with specific NDCs.*

FDA Label Image

Serialized Label (51662 1661 1)

A product label for AUVI-Q injection, solution, 0.1 mg/0.1 mL, distributed by HF Acquisitions Co., LLC, Mukilteo, WA. The label includes numeric codes likely representing product identification and manufacturing data, along with a Data Matrix barcode and the text 'SEE MANUFACTURE'S INSERT'.*

FDA Label Image

Serialized Label (51662 1661 2)

A white rectangular label featuring printed lines of code numbers in black, including a GS1 DataMatrix barcode on the right side. The text includes references to the manufacturer, HF Acquisitions Co., LLC in Mukilteo, WA, and notes to see the manufacturer's insert. The label also includes 'RX ONLY' printed vertically next to the 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.