Zafirlukast Tablet, Film Coated
Product Images NDC 55111-625

4 FDA label images from Dr. Reddys Laboratories Limited · 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 Zafirlukast (NDC 55111-625). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddys Laboratories Limited, 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

Container1

Container1
Zafirlukast Tablets 10 mg film-coated tablets label from Dr. Reddys Laboratories Limited. The label states 60 tablets per container with NDC 55111-625-60, emphasizes dispensing in the original airtight container, and provides regulatory and storage information. It includes a QR code and a barcode for tracking.*
FDA Label Image

Container2

Container2
Label for Zafirlukast Tablets 20 mg, a human prescription drug by Dr. Reddys Laboratories Limited. The label indicates 60 film-coated tablets for oral use. Includes dosage instructions, storage conditions, pharmacist dispensing notes, a barcode, and a QR code for patient information.*
FDA Label Image

Graph (Graph)

Graph (Graph)
A line graph showing mean ß2-agonist use (puffs per day) over a 14-week trial period. The graph compares placebo, Zafirlukast 20 mg twice daily, and Cromolyn sodium 1600 mcg four times a day, with ß2-agonist use on the vertical axis and trial week on the horizontal axis.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Zafirlukast, depicting its molecular arrangement with rings, methyl groups, and sulfonamide moiety, consistent with the active ingredient in the Zafirlukast tablets by Dr. Reddys Laboratories Limited.*

* 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.