Zithromax Injection, Powder, Lyophilized, For Solution
Product Images NDC 0069-3150

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zithromax (NDC 0069-3150). 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 Iv 01)

Chemical structure diagram of azithromycin dihydrate, the active ingredient in Zithromax injection. The diagram depicts the molecular arrangement of atoms and bonds in the azithromycin molecule, showing detailed ring and side chain structures.*

FDA Label Image

Logo (Zithromax Iv 02)

FDA Label Image

Principal Display Panel (500 mg Vial Label)

Label of Zithromax 500 mg/vial injection, powder, lyophilized for intravenous use. The label shows the product name and strength prominently with the NDC 0069-3150-84. It includes storage instructions, usage directions, and dilution requirements. Distributed by Pfizer Labs, it also notes the product is sterile, Rx only, and contains no latex or preservative.*

FDA Label Image

Principal Display Panel (10 Vials Carton)

Packaging label for Zithromax (azithromycin) injection 500 mg/vial, a sterile lyophilized powder for intravenous infusion. The label indicates the product contains 10 single-dose vials, is preservative-free, and manufactured by Pfizer Laboratories Div Pfizer Inc. The label includes directions for reconstitution and barcodes, with a design featuring blue and black patterns.*

* 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.