Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 70518-3933

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 70518-3933). 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

Remedy_label (Remedy Label)

Label for Quetiapine Fumarate 400 mg film-coated tablets by RemedyRepack Inc. The label indicates a quantity of 30 tablets and includes dosing form as oral tablets. Manufacturer is noted as Aurobindo Pharma, Dayton, NJ. The label features barcode, QR code, and storage instructions (20-25°C). It is marked as Rx only.*

FDA Label Image

Figure1 (Quetiapine Fig1)

A Kaplan-Meier curve chart illustrating the time to recurrence of a mood event in a clinical study. The x-axis represents time in weeks, and the y-axis shows the proportion of patients with relapse in percentage. Two survival curves are displayed, comparing patients treated with Quetiapine Fumarate plus lithium/valproate versus placebo plus lithium/valproate.*

FDA Label Image

Figure2 (Quetiapine Fig2)

Kaplan-Meier curves illustrating the proportion of patients experiencing relapse over time in weeks. The graph compares two groups: one receiving QTP+L/VAL and the other receiving PLA+L/VAL, showing relapse rates up to 100 weeks.*

FDA Label Image

Chemical Structure (Quetiapine Str)

Chemical structure of Quetiapine Fumarate, showing the molecular arrangement of quetiapine linked with fumarate, including nitrogen, oxygen, sulfur atoms, and ring structures distinct to the compound.*

* 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.