Montelukast Sodium Tablet, Film Coated
Product Images NDC 68071-4047

3 FDA label images from Nucare Pharmaceuticals,inc. · 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 Montelukast Sodium (NDC 68071-4047). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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.

FDA Label Image

68071 4047 3

68071 4047 3
Montelukast Sodium 10 mg oral film-coated tablets label from NuCare Pharmaceuticals, Inc., NDC 68071-4047. The label indicates a quantity of 30 tablets, RX Only, with manufacturing information from Intas Pharmaceuticals Limited, India. It includes warnings, storage instructions, and barcode details on a predominantly white label with blue and black text.*
FDA Label Image

Image Of Figure 1 (Montelukast Fig1)

Image Of Figure 1 (Montelukast Fig1)
A line graph showing mean percent change from baseline over weeks in treatment for Montelukast Sodium Tablets (10 mg) versus placebo. The x-axis represents weeks in treatment with a washout phase after 12 weeks, and the y-axis represents mean percent change from baseline. The Montelukast group shows a higher increase compared to placebo throughout the treatment period.*
FDA Label Image

Image Of Chemical Structure (Montelukast Str)

Image Of Chemical Structure (Montelukast Str)
Chemical structure of Montelukast Sodium showing its molecular framework including a chloro-substituted quinoline ring, a cyclopropyl carboxylate group, and other characteristic functional groups.*

* 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.