Azithromycin Dihydrate Tablet
Product Images NDC 80425-0412

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Azithromycin Dihydrate (NDC 80425-0412). 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)

Chemical structure of azithromycin dihydrate, showing its molecular arrangement with multiple rings and functional groups typical of this macrolide antibiotic compound.*

FDA Label Image

Image (1ede87c9 811c 4887 A274 A248a1e58a9d 02)

Instructions for removing azithromycin tablets from blister packaging in 250 mg and 500 mg strengths. Both show peeling the paper from perforated sections to expose foil, then pushing the tablet through the foil. The illustrations demonstrate manual steps for safe and easy tablet extraction.*

FDA Label Image

Azithromycin 500mg #3 (Azithromycin 500mg 80425 0412 01)

Label for azithromycin dihydrate 500 mg oral tablet by Advanced Rx of Tennessee, LLC, Nashville, TN. Includes product NDC 80425-041-01 and mentions comparison to Zithromax. The label shows storage instructions, lot number, and expiration date 6/30/2025. Manufacturer name Lupin Pharma is partially visible along with lot and serial numbers.*

* 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.