Montelukast Tablet, Film Coated
Product Images NDC 82009-009

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Montelukast (NDC 82009-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quallent Pharmaceuticals Health 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

Figure1.jpg (Figure1)

Chemical structure of Montelukast sodium, depicting its molecular arrangement including a chlorophenyl group, benzene rings, a cyclopropane ring, sulfur, and sodium carboxylate group as part of the compound.*

FDA Label Image

Figure2.jpg (Figure2)

A line graph showing mean percent change from baseline over weeks of treatment for Montelukast Sodium and placebo. The x-axis represents weeks of treatment from 0 to 15, including a washout period. The y-axis represents mean percent change, ranging from 0 to 15. Data points are marked with symbols for Montelukast Sodium and placebo, with Montelukast showing higher mean percent change throughout treatment.*

FDA Label Image

Montelabel1000s (Montelabel1000s)

Montelukast Sodium Tablets, USP 10 mg film-coated tablet label by Quallent Pharmaceuticals Health LLC. The label includes the NDC number 82009-009-10, storage instructions at 20° to 25°C, a warning to protect from moisture and light, medication guide availability, and manufacturer information including HETERO Labs Limited, India. It specifies 1000 tablets per container and Rx only status.*

FDA Label Image

Quallent-logo2 (Quallent Logo1 Copy)

FDA Label Image

Quallent-logo1 (Quallent Logo1)

* 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.