Auvi-q Injection, Solution
Product Images NDC 51662-1661
View Photos of Packaging, Regulatory Labels, and Product Appearance
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.
How Supplied (51662 1661 How Supplied)
This text provides information about the package configurations and strengths of autoinjectors along with their corresponding National Drug Codes (NDC). Different doses of autoinjectors are listed, such as 0.3mg, 0.15mg, and 0.1mg, each associated with a specific NDC number. This data can be used by healthcare professionals, pharmacists, and patients to accurately identify and dispense the correct medication.*
Serialized Label (51662 1661 1)
Serialized Label (51662 1661 2)
This is a product identification number found on a label or packaging. It indicates the manufacturer's reference number and suggests that further information can be found in the manufacturer's insert. The product is distributed by HF Acquisitions Co., LLC in Mukilteo, WA. The text also includes a note that the product is for prescription use only.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.