Azithromycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 55150-174

3 FDA label images from Eugia Us Llc · 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 Azithromycin (NDC 55150-174). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, 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

Package Label-principal Display Panel (500 mg per vial)

Package Label-principal Display Panel (500 mg per vial)
Label for Azithromycin for Injection, USP, 500 mg per vial, lyophilized powder for intravenous infusion only. Distributed by AuroMedics Pharma LLC. The label notes that the product must be further diluted before use and is sterile for prescription use only. The label includes storage instructions and a barcode.*
FDA Label Image

Package Label-principal Display Panel (500 mg per vial)

Package Label-principal Display Panel (500 mg per vial)
Packaging label for Azithromycin for Injection, USP 500 mg per vial, intravenous lyophilized powder for solution by Eugia US LLC. The carton contains 10 vials and states the product must be further diluted before use. Distributed by AuroMedics Pharma LLC, made in India, the label includes reconstitution and storage details.*
FDA Label Image

Azithromycin Chemical Structure (Azithromycin Str)

Azithromycin Chemical Structure (Azithromycin Str)
Chemical structure of Azithromycin, a macrolide antibiotic. The diagram shows the multi-ring lactone structure with attached methyl, hydroxyl, and amine functional groups characteristic of Azithromycin.*

* 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.