Azithromycin Dihydrate Tablet
Product Images NDC 80425-0431

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Azithromycin Dihydrate (NDC 80425-0431). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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 (1ede87c9 811c 4887 A274 A248a1e58a9d 01)

Structure (1ede87c9 811c 4887 A274 A248a1e58a9d 01)
Chemical structure of azithromycin dihydrate, a macrolide antibiotic. The diagram depicts the molecular arrangement of atoms and bonds that make up the active ingredient azithromycin dihydrate in the product.*
FDA Label Image

Image (1ede87c9 811c 4887 A274 A248a1e58a9d 02)

Image (1ede87c9 811c 4887 A274 A248a1e58a9d 02)
Illustrations showing how to open azithromycin tablets in two strengths, 250 mg and 500 mg. Each set of three panels demonstrates tearing along the perforation to separate the blister, peeling back the paper to expose the foil, and pushing the tablet through the foil for oral administration.*
FDA Label Image

Blister Card (250 mg)

Blister Card (250 mg)
Packaging label for azithromycin dihydrate 250 mg oral tablets, distributed by Advanced Rx of Tennessee, LLC. The label sheet contains multiple small patient blister pack inserts, each with dosage instructions for a 5-day course, including text and barcodes on a white background with pink and black borders.*
FDA Label Image

Azithromycin 250mg #6 (Azithromycin 250mg 80425 0431 01)

Azithromycin 250mg #6 (Azithromycin 250mg 80425 0431 01)
Label for azithromycin dihydrate 250 mg oral tablet from Advanced Rx of Tennessee, LLC. The label includes storage instructions (20°-25°C), the proprietary name, dosage strength, and a barcode. It also references comparison to Zithromax with related NDC and lot expiration details, and indications for prescription use only.*

* 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.