Azithromycin Monohydrate
Product Images NDC 53217-403

View Photos of 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 Monohydrate (NDC 53217-403). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals 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

Structure (Azithromycin 500mg 1)

Structure (Azithromycin 500mg 1)
Chemical structure of azithromycin monohydrate, showing its macrocyclic lactone ring and associated sugar moieties.*
FDA Label Image

Image (Azithromycin 500mg 2)

Image (Azithromycin 500mg 2)
Instructional diagram showing how to open azithromycin tablets blister packs for 250 mg and 500 mg doses. Steps include tearing along the perforation to separate packaging, peeling back paper to expose foil, and pushing the tablet through the foil blister. The left column illustrates the 250 mg tablet process, and the right column shows the 500 mg tablet process.*
FDA Label Image

53217-0403_azithromycin_500mg (Azithromycin 500mg 3)

53217-0403_azithromycin_500mg (Azithromycin 500mg 3)
Label for Azithromycin USP tablets, 500 mg strength, in a 3-pack configuration. The label states each tablet contains azithromycin monohydrate equivalent to 500 mg azithromycin, film-coated, with dosage instructions partially printed. The product is labeled as generic for azithromycin, packaged by Aidarex Pharmaceuticals LLC, and includes NDC 53217-0403-01 with manufacturer Lupin Limited, India.*

* 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.