Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 70518-4705

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 70518-4705). 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)

Quetiapine Fumarate 25 mg oral film-coated tablets packaging label containing 30 tablets. The label shows the NDC 70518-4705-00 and indicates repackaging by RemedyRepack Inc., Indiana, PA. The manufacturer is Camber Pharma, Inc., Piscataway, NJ. Additional storage information and dosage instructions are referenced to the insert.*

FDA Label Image

Quetiapinetabs-fig-1 (Quetiapinetabs Fig 1)

A line graph showing the proportion of patients with relapse (%) over time in weeks. The graph compares two groups: QTP + LI/VAL represented by a dashed line, and PLA + LI/VAL represented by a solid line, with the percentage of relapse increasing over approximately 90 weeks.*

FDA Label Image

Quetiapinetabs-fig-2 (Quetiapinetabs Fig 2)

A Kaplan-Meier curve chart showing the proportion of patients with relapse over time in weeks. Two lines compare groups labeled 'GTP+ LINAL' and 'PLA+ LINAL,' with the y-axis representing the percentage of patients with relapse from 0 to 100% and the x-axis ranging from 0 to 100 weeks.*

FDA Label Image

Quetiapinetabsstructure (Quetiapinetabsstructure)

Chemical structure of quetiapine fumarate, showing the two main molecular components with the quetiapine moiety and fumarate moiety depicted in a structural formula diagram.*

* 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.