Montelukast Sodium
Product Images NDC 64205-655

4 FDA label images from Readymeds · 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 Montelukast Sodium (NDC 64205-655). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Readymeds, 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

Figure 1 (Montelukast Sodium 1)

Figure 1 (Montelukast Sodium 1)
A line graph showing change in height (cm) over weeks on treatment with three groups: SINGULAIR 5 mg, Beclomethasone 336 mcg, and placebo. The x-axis represents weeks from -18 to 58, and the y-axis shows change in height from -3 to 7 cm. The graph indicates comparative height changes among the treatment groups over time.*
FDA Label Image

Structural Formula (Montelukast Sodium 2)

Structural Formula (Montelukast Sodium 2)
Chemical structure of Montelukast Sodium, showing its molecular configuration including aromatic rings, a sodium carboxylate group, chlorine atom, and other functional groups characteristic of the compound.*
FDA Label Image

Figure 2 (Montelukast Sodium 3)

Figure 2 (Montelukast Sodium 3)
Line chart showing mean percent change from baseline over weeks in treatment, comparing placebo and Singulair. The y-axis represents mean percent change from baseline, and the x-axis shows weeks in treatment from 0 to 15. The chart illustrates treatment response trends for the two groups over time.*
FDA Label Image

Photo (Photo)

Photo (Photo)
Packaging label for Montelukast Sodium 10 mg tablets by ReadyMeds. The label shows a quantity of 30 tablets, NDC 64205-655-30, an expiration date of 12/2015, and lot number 3118332.*

* 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.