Azithromycin
Product Images NDC 0409-0144

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Azithromycin (NDC 0409-0144). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Figure 1 (Azithromycin 01)

Figure 1 (Azithromycin 01)
An instructional diagram illustrating a hand turning the cap of a medication bottle, with a directional arrow indicating a twist motion to open or close the bottle, labeled as Figure 1.*
FDA Label Image

Figure 2 (Azithromycin 02)

Figure 2 (Azithromycin 02)
An instructional illustration showing the removal of a cap from a container. The image depicts a hand lifting the cap upward from the bottle neck, indicating the method to open the container, presumably for Azithromycin labeled by Hospira, Inc.*
FDA Label Image

Figure 3 (Azithromycin 03)

Figure 3 (Azithromycin 03)
Illustration showing a hand holding and removing the cap from a rectangular bottle or vial, depicting a step in accessing the product inside. The figure is labeled as 'Figure 3'.*
FDA Label Image

Figure 4 (Azithromycin 04)

Figure 4 (Azithromycin 04)
An instructional illustration showing a hand manipulating a mechanism on a flexible medical pouch or bag. The image appears to demonstrate the proper way to open or adjust a component on the pouch, likely related to fluid administration.*
FDA Label Image

Figure 5 (Azithromycin 05)

Figure 5 (Azithromycin 05)
An instructional line drawing labeled 'Figure 5' depicts hands manipulating a medical vial or container, showing how to handle or extract fluid with a stopper or seal mechanism. The image is likely intended to demonstrate proper use or preparation technique for a liquid pharmaceutical product.*
FDA Label Image

Figure 6 (Azithromycin 06)

Figure 6 (Azithromycin 06)
An instructional diagram showing hands holding and operating a liquid medication pouch with a cap, demonstrating proper preparation or use steps for the product Azithromycin by Hospira, Inc. The illustration highlights how to handle the pouch and secure the cap before administration.*
FDA Label Image

Figure 7 (Azithromycin 07)

Figure 7 (Azithromycin 07)
An instructional illustration showing a hand holding a rectangular medical bag with tubing and a central circular component, labeled as Figure 7. The image likely demonstrates a step in handling or using the product container.*
FDA Label Image

Azithromycin Structural Formula (Azithromycin 08)

Azithromycin Structural Formula (Azithromycin 08)
Chemical structure diagram of azithromycin, illustrating its molecular composition and arrangement with rings, methyl groups, hydroxyl groups, and nitrogen atoms.*
FDA Label Image

Hospira Logo (Azithromycin 09)

FDA Label Image

Principal Display Panel (500 mg Vial Label)

Principal Display Panel (500 mg Vial Label)
Label for Azithromycin for Injection, USP, 500 mg/vial by Hospira, Inc. This single-dose ADD-Vantage vial is sterile and intended for intravenous use. The label includes storage instructions, dosage form, and distributor information with NDC 0409-0144-21.*
FDA Label Image

Principal Display Panel (500 mg Vial Tray)

Principal Display Panel (500 mg Vial Tray)
Azithromycin for Injection, USP 500 mg/vial single-dose injectable vial packaging label by Hospira, Inc. The label states the product is for intravenous use and sterile. The package contains 10 single-dose ADD-Vantage vials. Additional storage and usage directions are printed on the label, along with barcodes and manufacturing details.*

* 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.