Quetiapine Fumarate Tablet
Product Images NDC 50268-635

9 FDA label images from Avpak · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine Fumarate (NDC 50268-635). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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 5026863015 Quetiapine 25mg 2016

Label 5026863015 Quetiapine 25mg 2016
Packaging label for Quetiapine Fumarate Tablets, USP 25 mg oral tablets by AvPAK. The label indicates Rx only and a package containing 50 tablets (5 bottles of 10 unit dose). Includes barcode, NDC 50268-630-15, storage instructions, warnings, and manufacturer information.*
FDA Label Image

Label 5026863115 Quetiapine 50mg 2016

Label 5026863115 Quetiapine 50mg 2016
Quetiapine Fumarate Tablets USP 50 mg oral tablets, labeled for prescription use only. Each package contains 50 tablets in 5 blister packs of 10 tablets each. The label includes the NDC number 50268-631-15 and identifies AvPAK as the manufacturer.*
FDA Label Image

Label 5026863215 Quetiapine 100mg 2016

Label 5026863215 Quetiapine 100mg 2016
Quetiapine Fumarate Tablets USP 100 mg oral tablets packaging label by AvPAK. The label indicates a 50 tablet count (5 strips of 10 tablets each), with an NDC code 50268-632-15. The label includes dosage strength, tablet form, storage instructions, and safety warnings for pediatric use.*
FDA Label Image

Label 5026863315 Quetiapine 200mg 2016

Label 5026863315 Quetiapine 200mg 2016
Label for Quetiapine Fumarate Tablets, USP, 200 mg strength, oral tablet dosage form. The label indicates the product is Rx only and contains 50 tablets (5 x 10 unit dose) packaged by AvPAK. The label includes storage instructions, a pharmacist directive, a warning to keep out of reach of children, and barcode.*
FDA Label Image

Label 5026863415 Quetiapine 300mg 2018

Label 5026863415 Quetiapine 300mg 2018
Quetiapine Tablets USP 300 mg oral tablets packaging label from AvPAK. The label shows 50 tablets in unit dose packaging (5 x 10) with NDC 50268-634-15. The label includes storage instructions, pharmacist dispensing guidance, and manufacturer information for AvKARE, Inc. from Pulaski, TN.*
FDA Label Image

Label 5026863515 Quetiapine 400mg 2016

Label 5026863515 Quetiapine 400mg 2016
Quetiapine Fumarate Tablets, USP 400 mg oral tablets, labeled by AvPAK. The label shows 50 tablets (5 x 10 unit dose) with the National Drug Code (NDC) 50268-635-15. It includes pharmacist instructions, storage conditions, and security warnings. The package is designated for prescription use only (Rx Only).*
FDA Label Image

Figure 1 (Quetiapine Fig1)

Figure 1 (Quetiapine Fig1)
A Kaplan-Meier curve showing the proportion of patients with relapse of a mood event over time in weeks. Two treatment groups are compared: QTP + LI/VAL (quetiapine fumarate plus lithium/valproate) and PLA + LI/VAL (placebo plus lithium/valproate). The graph depicts the relapse rates up to 100 weeks, indicating differences between the treatments.*
FDA Label Image

Figure 2 (Quetiapine Fig2)

Figure 2 (Quetiapine Fig2)
A Kaplan-Meier curve showing time to recurrence of a mood event over 100 weeks. The y-axis represents the proportion of patients with relapse (%), and the x-axis shows time (weeks). Two curves compare QTP+LIVAL and PLA+LIVAL groups, depicting the proportion of relapses over time in a clinical study.*
FDA Label Image

Structure (Quetiapine Stru)

Structure (Quetiapine Stru)
Chemical structure of quetiapine fumarate, showing the molecular arrangement of atoms including rings, nitrogen, oxygen, and sulfur components characteristic of quetiapine, paired with the fumarate moiety.*

* 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.