Montelukast Tablet
Product Images NDC 68071-3855

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Montelukast (NDC 68071-3855). 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

Pdp (68071 3855 3)

Montelukast Sodium 10 mg tablets packaging label from NuCare Pharmaceuticals, Inc. The label states #30 tablets per package and specifies that each film-coated tablet contains Montelukast Sodium USP equivalent to 10 mg Montelukast. It includes NDC 68071-3855-3 and storage instructions at controlled temperature 68-77°F. The label features manufacturer and packaging information, lot, expiry, and serial numbers, along with a warning to keep out of reach of children.*

FDA Label Image

Montelukast-fig-1 (Montelukast Fig 1)

A line graph showing mean percent change from baseline over weeks in treatment for Montelukast Sodium and placebo groups. The x-axis represents weeks in treatment from 0 to 15, including a washout period after week 12. The y-axis shows mean percent change from baseline, ranging from 0 to 15. Montelukast Sodium data points (black circles) show a higher mean percent change compared to placebo (white squares) across the treatment period, with values peaking around week 12 and declining during washout.*

FDA Label Image

Montelukast-structural (Montelukast Structural)

Chemical structure of Montelukast, showing its arrangement of aromatic rings, chlorine atom, sulfur linkage, cyclopropyl group, carboxylate sodium salt, and hydroxyl and methyl 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.