Zithromax Injection, Powder, Lyophilized, For Solution
Product Images NDC 0069-0400

4 FDA label images from Pfizer Laboratories Div Pfizer Inc · 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 Zithromax (NDC 0069-0400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer Inc, 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

Chemical Structure (Zithromax 01)

Chemical Structure (Zithromax 01)
Chemical structure diagram of azithromycin dihydrate, showing its molecular components and bonds in detail.*
FDA Label Image

Logo (Zithromax 02)

FDA Label Image

Principal Display Panel (500 mg Vial Label)

Principal Display Panel (500 mg Vial Label)
Label for Zithromax (azithromycin) injection, powder, lyophilized for solution, 500 mg per vial. The label indicates the product is a single-dose vial for intravenous infusion, sterile, with no latex and no preservative. It includes storage instructions, dilution directions, and notes the product is distributed by Pfizer Laboratories Division, Pfizer Inc.*
FDA Label Image

Principal Display Panel (500 mg Vial Carton)

Principal Display Panel (500 mg Vial Carton)
Packaging label for Zithromax injection, 500 mg/vial (azithromycin dihydrate) powder, lyophilized for solution. The label indicates a 10 single-dose vial carton, sterile for intravenous infusion, with no latex or preservative. Distributed by Pfizer Labs, with directions for reconstitution and storage instructions included on the label.*

* 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.