Clarithromycin Tablet, Film Coated, Extended Release
Product Images NDC 62135-883

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 Clarithromycin (NDC 62135-883). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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

Image Description (Clarithromycin Er Tablets 500 mg Bottle Label)

Image Description (Clarithromycin Er Tablets 500 mg Bottle Label)
The label for Clarithromycin Extended-Release Tablets, USP, 500 mg, film-coated tablets in a 60-tablet bottle from Chartwell Rx, LLC. It includes storage instructions, dosage warnings, manufacturer details, and a barcode. The label also states this is a prescription-only drug and cautions to keep all medications out of the reach of children.*
FDA Label Image

Image Description (Clarithromycin Er Tablets 500 mg Graph 1)

Image Description (Clarithromycin Er Tablets 500 mg Graph 1)
A line graph comparing mean plasma concentration (mcg/mL) over 24 hours after dosing for Clarithromycin extended-release (2 x 500 mg every 24 hours) and Clarithromycin (500 mg every 12 hours). The x-axis represents time after dosing in hours; the y-axis represents mean plasma concentration in mcg/mL.*
FDA Label Image
FDA Label Image

Image Description (Clarithromycin Er Tablets 500 mg Structure)

Image Description (Clarithromycin Er Tablets 500 mg Structure)
Chemical structure of clarithromycin, showing its detailed molecular arrangement with various functional groups including hydroxyl, methoxy, and methyl groups as well as the macrolide ring system.*

* 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.