Clarithromycin Tablet, Film Coated, Extended Release
Product Images NDC 0527-1930

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clarithromycin (NDC 0527-1930). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Clarithromycin Extended-release Tablets Usp, 500 mg (Clar Er Container Label 500mg)

Label for Clarithromycin Extended-Release Tablets, USP 500 mg, manufactured for Lannett Company, Inc. The label includes the NDC number 0527-1930-06 and features a white, oblong film-coated tablet with the imprint 'S58'. The package contains 60 tablets and indicates the product is for prescription use only. Storage and dosage instructions are also visible, along with manufacturer and distributor information.*

FDA Label Image

Chemical Structure For Clarithromycin (Clarithromycin Tab Stucture)

Chemical structure of Clarithromycin, showing its detailed molecular arrangement with multiple rings and attached functional groups including methyl, hydroxyl, and methoxy substituents.*

FDA Label Image

Steady State Graph (Clarithromycin Tabs Steady Graph)

A line graph comparing mean plasma concentration (mcg/mL) of clarithromycin over 24 hours after dosing. Two series are shown: clarithromycin extended-release (2 x 500 mg every 24 hours) represented by circles, and clarithromycin immediate release (500 mg every 12 hours) represented by triangles. The x-axis shows time after dosing in hours, and the y-axis shows mean plasma concentration in mcg/mL.*

FDA Label Image

Logo (Logo0001 01)

* 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.