Auvi-q Injection, Solution
Product Images NDC 51662-1662

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Auvi-q (NDC 51662-1662). 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 formula of the active ingredient in AUVI-Q injection solution, .15 mg/.15 mL strength. The structure features a benzene ring with hydroxyl groups and other molecular components consistent with epinephrine.*

FDA Label Image

How Supplied (51662 1661 How Supplied)

A data table presenting package configurations, strengths, and National Drug Codes (NDC) for AUVI-Q autoinjectors. Configurations include single and double autoinjector packages with strengths of 0.1 mg, 0.15 mg, and 0.3 mg, alongside corresponding unique NDC numbers for each.*

FDA Label Image

Serialized Label (51662 1662 1)

The image shows a label for AUVI-Q injection solution .15 mg/.15 mL by HF Acquisition Co LLC. It includes a Data Matrix barcode on the right and human-readable text with GS1 Application Identifiers providing product codes and dates. The label instructs to see the manufacturer's insert and lists the distributor's address in Mukilteo, WA 98275.*

FDA Label Image

Serialized Label (51662 1662 2)

A white label containing GS1 barcode data strings and a 2D barcode on the right. The text includes several numerical codes and states "SEE MANUFACTURE'S INSERT." The label also notes distribution by HF Acquisitions Co., LLC, Mukilteo, WA 98275. No product name or dosage information is visible.*

* 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.