Quetiapine Fumarate Tablet, Film Coated
Product Images NDC 50090-6337

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 50090-6337). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 Image (Lbl500906337)

Label Image (Lbl500906337)
Quetiapine Fumarate 400 mg film-coated oral tablets label from A-S Medication Solutions. The label states each film-coated tablet contains 400 mg of quetiapine fumarate with a package size of 30 tablets. Storage instructions recommend 68 to 77 degrees Fahrenheit. The label includes NDC 50090-6337, a QR code, and Reorder number 65862-495-01.*
FDA Label Image

Figure1 (Quetiapine Fig1)

Figure1 (Quetiapine Fig1)
A Kaplan-Meier curve chart depicting the proportion of patients with relapse over time in weeks. Two groups are compared: one labeled QTP+LI/VAL and the other PLA+LI/VAL, showing differences in relapse rates up to 100 weeks.*
FDA Label Image

Figure2 (Quetiapine Fig2)

Figure2 (Quetiapine Fig2)
A Kaplan-Meier curve graph showing the proportion of patients with relapse of a mood event over time in weeks, comparing two groups labeled QTP+L/VAL and PLA+L/VAL. The vertical axis represents the percentage of patients with relapse, and the horizontal axis represents time in weeks, up to 100 weeks.*
FDA Label Image

Chemical Structure (Quetiapine Str)

Chemical Structure (Quetiapine Str)
Chemical structure of Quetiapine Fumarate showing the molecular arrangement of its components, including key cyclic and functional groups, consistent with the active ingredient Quetiapine Fumarate.*

* 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.