Zafirlukast Tablet, Coated
Product Images NDC 64380-187

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 Zafirlukast (NDC 64380-187). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science 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

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Chemical structure of zafirlukast, the active ingredient in Zafirlukast tablets, showing its molecular components and bonds.*
FDA Label Image

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A line graph comparing mean beta-2 agonist use (puffs per day) over a 14-week trial period across three groups: placebo, Zafirlukast 20 mg twice daily, and Cromolyn sodium 1600 µg four times a day. The y-axis represents adjusted treatment means of puffs per day, and the x-axis shows trial weeks.*
FDA Label Image

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Label for Zafirlukast Tablets 10 mg by Strides Pharma Inc. The label includes dosage warnings, storage instructions, and states the package contains 60 coated tablets. It features the strength prominently in pink and indicates prescription use only. The label also shows a barcode and distributor information for Strides Pharma Inc., East Brunswick, NJ.*
FDA Label Image

20 mg (label)

20 mg (label)
Label for Zafirlukast Tablets 20 mg oral coated tablets by Strides Pharma Science Limited. The label includes dosage warnings, storage instructions, quantity of 60 tablets, and a barcode. The label emphasizes dispensing in the original airtight container and is marked Rx only.*

* 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.