Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 70518-3609

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 70518-3609). 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 300 mg film-coated tablets, oral use, in a package containing 30 tablets. The label includes the NDC 70518-3609-00 and states it is repackaged by RemedyRepack Inc. It shows manufacturer information for Rising Pharma, Inc., and storage directions. The label is primarily white and purple with RemedyRepack branding.*

FDA Label Image

Figure1 (Quetiapine Fig1)

A Kaplan–Meier curve graph showing the proportion of patients with relapse over time in weeks, comparing two groups labeled QTP+LI/VAL and PLA+LI/VAL from Study 7. The x-axis represents time in weeks up to 100, and the y-axis shows the percentage of patients with relapse, ranging from 0 to 100%.*

FDA Label Image

Figure2 (Quetiapine Fig2)

A Kaplan-Meier curve graph showing time to recurrence of a mood event in a study. The graph plots the proportion of patients with relapse (%) on the y-axis against time in weeks on the x-axis. Two curves are shown: one labeled QTP+LI/VAL (dashed line) and the other PLA+LI/VAL (solid line), comparing relapse rates over 100 weeks.*

FDA Label Image

Chemical Structure (Quetiapine Str)

Chemical structure of quetiapine fumarate, showing the molecular arrangement of quetiapine linked to fumarate ions. The image depicts the chemical bonds and ring structures characteristic of this 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.