Quetiapine Tablet, Extended Release
Product Images NDC 71335-2641

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Quetiapine (NDC 71335-2641). 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

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Chemical structure diagram showing the molecular formula of Quetiapine fumarate, the active ingredient in the Quetiapine 400 mg extended release tablets by Bryant Ranch Prepack.*

FDA Label Image

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A line graph depicting the proportion of patients with relapse (%) over time in months up to 7 months. Two lines are shown: a dashed line representing PLA and a solid line representing QTP XR. The graph illustrates a higher relapse rate over time for PLA compared to QTP XR.*

FDA Label Image

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A line graph depicting the proportion of patients with relapse (%) over time (weeks). It compares two groups, one labeled "QTP + LIVAL" and the other "PLA + LIVAL," showing relapse curves with different relapse rates over time up to 100 weeks.*

FDA Label Image

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This is a line graph depicting the proportion of patients with relapse (%) on the y-axis against time in weeks on the x-axis. It compares two groups labeled QTP+ LI/VAL and PLA+ LI/VAL, showing relapse proportions over a 100-week period.*

FDA Label Image

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FDA Label Image

Label (Lbl713352641)

Label for Quetiapine Extended-Release Tablets USP, 400 mg, repackaged by Bryant Ranch Prepack and manufactured by Unichem Laboratories Ltd. The label shows a quantity of 60 tablets, storage conditions, a QR code for prescribing information, and warnings.*

* 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.