Azithromycin Dihydrate Tablet, Film Coated
Product Images NDC 83112-501

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Azithromycin Dihydrate (NDC 83112-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Health Department, Oklahoma State, 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

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Azithromycin Dihydrate 500 mg film-coated oral tablets. Each pink, oblong tablet is imprinted with "QE" on one side and "500" on the other. Labeler is Health Department, Oklahoma State. Product NDC: 83112-501.*

FDA Label Image

Azithromycin 500mg Ept (Azithromycin 500mg (ept))

Azithromycin Dihydrate 500 mg film coated tablets in a 2-count blister pack sealed inside a small clear plastic zip pouch. The pack has a bright pink label indicating the product name, strength, and tablet count. The image shows the oral dosage form with red tablets visible.*

FDA Label Image

Azithromycin 500mg 2-count (Azithromycin 500mg 2 Count (front))

Azithromycin Dihydrate 500 mg film-coated tablets, packaged as a 2-count blister sealed in a clear plastic bag. The bag features an orange label with text indicating 'STI Azithromycin 500 mg 2 CT.' This packaging is labeled by Health Department, Oklahoma State.*

FDA Label Image

Azithromycin 500mg 4-count (Azithromycin 500mg 4 Count (front))

Azithromycin 500 mg tablets in a blister pack partially visible inside a small clear resealable plastic bag. The white paper label on the bag reads 'STI Azithromycin 500mg 4 Tablets.' The tablets are oval and red, with four tablets visible. No manufacturer or NDC information is printed 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.