Azithromycin
Product Images NDC 33261-139

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 (NDC 33261-139). 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

50111078766

50111078766
Azithromycin tablets imprinted with "PLIVA" on one side and "787" on the other, in an elongated oval white form. The image includes measurement scales indicating the tablet size. Labeler information is Aidarex Pharmaceuticals LLC. Product NDC 33261-139.*
FDA Label Image

Structural Formula (Azithromycin 250mg 1)

Structural Formula (Azithromycin 250mg 1)
Chemical structure diagram of azithromycin, showing its detailed molecular framework with multiple rings and functional groups. The structure illustrates the arrangement of atoms and bonds typical for this macrolide antibiotic, corresponding to the active ingredient azithromycin in the drug product by Aidarex Pharmaceuticals LLC.*
FDA Label Image

33261-0139_azithromycin_250mg (Azithromycin 250mg 2)

33261-0139_azithromycin_250mg (Azithromycin 250mg 2)
Azithromycin USP 250 MG film-coated tablets, package containing 6 white oval tablets with imprint. The label indicates the active ingredient azithromycin monohydrate equivalent to azithromycin 250 mg. Manufactured by Pliva Hrvatska D.O.O. Croatia and labeled by Aidarex Pharmaceuticals LLC. The label includes lot number, expiration date, and multiple identifiers including NDC 33261-0139-06.*

* 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.