Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 50090-3983

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 50090-3983). 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 showing the molecular arrangement of the active ingredient including the quetiapine molecule and fumarate ion.*

FDA Label Image

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A line graph showing the proportion of patients with relapse (%) over time (weeks) up to 100 weeks. Two curves are displayed: one for QTP + LI/VAL (dashed line) and another for PLA + LI/VAL (solid line). The graph illustrates the relapse trends for these treatment groups over the study period.*

FDA Label Image

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A line graph depicting the proportion of patients with relapse (%) over time in weeks, comparing two groups: QTP+ LI/VAL and PLA+ LI/VAL. The graph shows an increasing relapse proportion for both groups, with QTP+ LI/VAL having a higher relapse rate compared to PLA+ LI/VAL over the duration of 100 weeks.*

FDA Label Image

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FDA Label Image

Label Image (Lbl500903983)

Quetiapine Fumarate 300 mg film-coated tablet label from A-S Medication Solutions. The label includes the NDC 50090-3983-0, storage instructions to keep at 68 to 77 degrees Fahrenheit, and a quantity of 60 tablets. It also mentions each film-coated tablet contains quetiapine fumarate USP equivalent to 300 mg quetiapine.*

* 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.