Clarithromycin
Product Images NDC 68180-177

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 68180-177). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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.

Product Images & Figures Index

FDA Label Image

Image-01 (Dc751b37 3923 4431 8378 C818a1f87689 01)

Image-01 (Dc751b37 3923 4431 8378 C818a1f87689 01)
Chemical structure of clarithromycin, showing its detailed arrangement of atoms and bonds including methyl, hydroxyl, and methoxy groups as part of its macrolide antibiotic molecular framework.*
FDA Label Image

Image-02 (Dc751b37 3923 4431 8378 C818a1f87689 02)

Image-02 (Dc751b37 3923 4431 8378 C818a1f87689 02)
A line graph comparing mean plasma concentration (mcg/mL) of Clarithromycin over 24 hours post-dosing. It shows two regimens: extended-release tablets 2x500 mg every 24 hours and standard tablets 500 mg every 12 hours, with plasma concentration on the y-axis and time after dosing in hours on the x-axis.*
FDA Label Image

Image02 (Dc751b37 3923 4431 8378 C818a1f87689 03)

Image02 (Dc751b37 3923 4431 8378 C818a1f87689 03)
Label for Clarithromycin Extended-release Tablets USP 500 mg by Lupin Pharmaceuticals, Inc. The label indicates each tablet contains 500 mg clarithromycin in an extended-release film-coated form, with 60 tablets in the package. It includes storage instructions, dosage guidance, and manufacturer details for Lupin Pharmaceuticals and Lupin Limited, along with an NDC barcode.*

* 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.