Quetiapine Fumarate
Product Images NDC 50090-4022

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 50090-4022). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 quetiapine fumarate, depicting the molecular arrangement and bonding for the active ingredient quetiapine fumarate as shown in the image.*

FDA Label Image

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A survival curve chart depicting the proportion of patients with relapse (%) over time in weeks. The chart compares two groups: one receiving QTP+LIVAL and the other PLA+LIVAL. The PLA+LIVAL group shows a higher and faster relapse rate, leveling off around 70%, while the QTP+LIVAL group shows a lower relapse rate, leveling off around 40% by week 100.*

FDA Label Image

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A line graph depicting the proportion of patients with relapse over time in weeks. The y-axis shows the proportion of patients with relapse as a percentage, while the x-axis shows time in weeks from 0 to 100. Two lines are shown: one solid line labeled QTP+LI/VAL and one dashed line labeled PLA+LI/VAL, indicating different treatment groups and their relapse rates over time.*

FDA Label Image

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FDA Label Image

Label Image (Lbl500904022)

Quetiapine Fumarate 50 mg tablet bottle label from A-S Medication Solutions. The label indicates the product NDC 50090-4022, contains 30 tablets, and states storage instructions to keep the tablets at 68 to 77 degrees Fahrenheit. The label also includes dosage directions and a QR code.*

* 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.