Quetiapine Fumarate Tablet
Product Images NDC 71335-2278

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 71335-2278). 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

Molecular Structure (E6dd3e1f 31d1 4d58 A717 D0bb4a4b8b6d 01)

Chemical structure diagram of quetiapine fumarate, showing the molecular components including the quetiapine moiety and fumarate ions as distinct parts of the combined structure.*

FDA Label Image

Figure 1 (E6dd3e1f 31d1 4d58 A717 D0bb4a4b8b6d 02)

A Kaplan-Meier type graph showing the proportion of patients with relapse (%) over time (weeks). Two lines compare relapse rates: a solid line for PLA+LI/VAL and a dashed line for QTP+LI/VAL, illustrating different relapse trends over approximately 100 weeks.*

FDA Label Image

Figure 2 (E6dd3e1f 31d1 4d58 A717 D0bb4a4b8b6d 03)

A line graph showing the proportion of patients with relapse (%) over time in weeks up to 100 weeks. It compares two treatments: a dashed line for QTP+LI/VAL and a solid line for PLA+LI/VAL, illustrating relapse proportion trends for each group.*

FDA Label Image

Label (Lbl713352278)

Label for Quetiapine Tablets USP 300 mg oral tablets shows NDC 71335-2278-1. The label states that each film-coated tablet contains 345.36 mg of Quetiapine Fumarate USP equivalent to 300 mg Quetiapine. The package contains 30 tablets and is repackaged by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Lupin Limited.*

* 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.