Quetiapine Fumarate Tablet
Product Images NDC 70518-2901

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 70518-2901). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

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Chemical structure diagram of quetiapine fumarate showing the detailed molecular arrangement of the active ingredient quetiapine and fumarate ions as represented in the product data.*

FDA Label Image

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A Kaplan-Meier plot showing the proportion of patients with relapse (%) on the y-axis over time (weeks) on the x-axis. Two treatment groups are compared: QTP + LI/VAL (dashed line) and PLA + LI/VAL (solid line). The plot illustrates relapse rates increasing over 100 weeks, with the PLA + LI/VAL group showing a higher relapse proportion than the QTP + LI/VAL group.*

FDA Label Image

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A Kaplan-Meier survival curve chart depicting the proportion of patients with relapse over time in weeks. Two groups are compared: QTP+LI/VAL (dashed line) and PLA+LI/VAL (solid line). The y-axis shows the proportion of patients with relapse as a percentage, ranging from 0 to 100%, while the x-axis represents time in weeks up to 100 weeks.*

FDA Label Image

Remedy_label (Remedy Label)

Label for Quetiapine fumarate 50 mg oral tablets, packaged in a quantity of 30. The label shows Quetiapine as the proprietary name. The labeler is RemedyRepack Inc., Indiana, PA. The original manufacturer is Lupin Pharma, Baltimore, MD. The label includes storage instructions 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.