Quetiapine Fumarate Tablet
Product Images NDC 82804-094

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 82804-094). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

82804-094-30 (Quetiapine 100 100 Tab A)

Label for Quetiapine 100 mg tablets by Proficient Rx LP. The package contains 30 yellow, round, biconvex film-coated tablets debossed with "261." Each tablet contains 115.13 mg quetiapine fumarate USP equivalent to 100 mg quetiapine. Manufactured by Alkem Laboratories Ltd., India. Storage instructions and multiple barcode labels with NDC 82804-094-30 shown.*

FDA Label Image

Quetiapine-fig1 (Quetiapine Fig1)

Kaplan-Meier curves showing time to recurrence of a mood event over approximately 100 weeks. The graph displays the proportion of patients with relapse (%) on the y-axis and time in weeks on the x-axis. Two curves compare QTP+ LI/VAL and PLA+ LI/VAL treatment groups, with QTP+ LI/VAL showing a lower relapse proportion over time.*

FDA Label Image

Quetiapine-fig2 (Quetiapine Fig2)

Kaplan-Meier curves showing the proportion of patients with relapse of a mood event over time in weeks. Two groups are compared: QTP+ LI/VAL (dashed line) and PLA+ LI/VAL (solid line). The graph illustrates time to recurrence with relapse percentages on the y-axis and time in weeks on the x-axis up to 100 weeks.*

FDA Label Image

Structure (Quetiapine Stru)

Chemical structure of Quetiapine Fumarate, showing the molecular arrangement of quetiapine with its fumarate salt form.*

* 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.