Clarithromycin Tablet, Film Coated
Product Images NDC 43063-823

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 Clarithromycin (NDC 43063-823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, Inc., 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

Image (43063823)

Image (43063823)
Label for Clarithromycin USP 500 mg oral film-coated tablets, packaged by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. The package contains 28 tablets. The label includes the National Drug Code (NDC) 43063-823-28, lot number H19B91, and expiration date 05/2021. It features warnings to keep out of reach of children, dosage and storage instructions, and directions for use in English and Spanish. The label also includes reorder information and a QR code.*
FDA Label Image

Figure 1 (Clarithromycin Fig1)

Figure 1 (Clarithromycin Fig1)
A survival curve chart showing the proportion surviving over days since randomization comparing Clarithromycin and placebo. The x-axis represents days since randomization (0 to about 700 days), and the y-axis shows the proportion surviving (from 0.0 to 1.0). Two lines represent Clarithromycin (solid line) and placebo (dashed line), illustrating differences in survival rates over time.*
FDA Label Image

Chemical Structure (Clarithromycin Str)

Chemical Structure (Clarithromycin Str)
Chemical structure of clarithromycin showing its molecular configuration with detailed rings and functional groups, consistent with the active ingredient clarithromycin.*

* 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.