Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 71335-2691

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 71335-2691). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label (Lbl713352691)

Quetiapine Fumarate 50 mg film-coated tablets label showing NDC 71335-2691-1. The label includes dosage strength, repackager Bryant Ranch Prepack, Inc., and manufacturer Aurobindo Pharma Limited. It states contents as 30 tablets and includes storage instructions and a QR code for package insert access.*

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 as a percentage. Two treatment groups are compared: one labeled QTP+LIVAL and the other PLA+LIVAL, with relapse proportions increasing over time for both groups.*

FDA Label Image

Figure2 (Quetiapine Fig2)

Kaplan-Meier curves chart displaying the proportion of patients with relapse over time in weeks. The chart compares relapse rates between two groups labeled QTP+LI/VAL and PLA+LI/VAL, with the y-axis representing the proportion of patients with relapse (%) and the x-axis showing time in weeks.*

FDA Label Image

Chemical Structure (Quetiapine Str)

Chemical structure diagram of Quetiapine Fumarate, showing the molecular arrangement of the quetiapine moiety bound with fumarate, represented as a complex molecule with rings and functional groups typical of the drug's composition.*

* 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.