Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 70518-2175

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 70518-2175). 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

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Chemical structure of quetiapine fumarate, showing the molecular configuration of the active ingredient quetiapine combined with fumarate.*
FDA Label Image

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A line graph showing the proportion of patients with relapse over time (weeks). Two curves compare relapse rates: one for QTP + LI/VAL (dashed line) and one for PLA + LI/VAL (solid line). The y-axis indicates the proportion of patients with relapse (%) ranging from 0 to 100, while the x-axis shows time in weeks from 0 to 100.*
FDA Label Image

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A line graph showing the proportion of patients with relapse over time in weeks. Two lines represent groups labeled as QTP+ LI/VAL and PLA+ LI/VAL, depicting their relapse rates increasing differently over approximately 100 weeks.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Label for Quetiapine Fumarate 50 mg film-coated tablets, oral administration. The label indicates a quantity of 30 tablets and is marked RX only. It includes a barcode, a QR code, and text advising to keep medication out of reach of children. Manufacturer listed as Unichem Pharma Inc., repackaged by RemedyRepack Inc., Indiana, PA.*

* 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.