Quetiapine Tablet, Film Coated
Product Images NDC 0093-8162

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine (NDC 0093-8162). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Quetiapine Fumarate Structural Formula (Image 1)

Chemical structure diagram showing the molecular structure of quetiapine fumarate, including the quetiapine moiety and fumarate salt components as displayed in the diagram.*

FDA Label Image

Figure 1 (Image 2)

A Kaplan-Meier survival curve chart showing the proportion of patients with relapse (%) on the y-axis versus time in weeks on the x-axis. Two lines compare relapse rates between QTP + LI/VAL and PLA + LI/VAL groups over approximately 90 weeks, with the QTP + LI/VAL group showing a lower proportion of relapse.*

FDA Label Image

Figure 2 (Image 3)

A line graph showing the proportion of patients with relapse (%) over time in weeks. Two groups are compared: one represented by a dashed line labeled "QTP+ LI/VAL" and the other by a solid line labeled "PLA+ LI/VAL." The graph depicts relapse proportions increasing over time for both groups, with the PLA+ LI/VAL group having a higher relapse rate throughout the 100-week period.*

FDA Label Image

Label-25mg (Image 4)

Quetiapine Tablets USP 25 mg tablet bottle label showing the product name, strength, quantity of 100 tablets, and manufacturer Teva Pharmaceuticals USA Inc. The label includes a barcode, NDC number 0093-2063-01, medication guide instructions, storage conditions, and a serialization coding area.*

FDA Label Image

Label-50mg (Image 5)

Quetiapine Tablets USP 50 mg tablet label from Teva Pharmaceuticals USA Inc. The label displays the drug name and strength prominently, along with directions for pharmacists to dispense the accompanying Medication Guide. It states the package contains 100 tablets, includes a barcode, serialization coding area, and storage instructions. Manufactured by Teva Pharmaceuticals USA Inc.*

FDA Label Image

Label-100mg (Image 6)

Quetiapine Tablets USP 100 mg tablet bottle label from Teva Pharmaceuticals USA Inc. The label includes the medication name, strength in milligrams, a pharmacist instruction to dispense the accompanying Medication Guide, quantity of 100 tablets, and relevant storage and safety information. The label also displays the NDC 0093-8162-01 and includes a serialization coding area.*

FDA Label Image

Label-200mg (Image 7)

Label for Quetiapine Tablets USP 200 mg by Teva Pharmaceuticals USA Inc. The label states a count of 100 tablets, includes NDC 0093-8163-01, dosing warnings, storage instructions, and pharmacist dispensing guidance. The label also displays the Teva logo and serialization coding area.*

FDA Label Image

Label-300mg (Image 8)

Quetiapine Tablets USP 300 mg tablet bottle label by Teva Pharmaceuticals USA Inc. The label includes NDC 0093-8164-01, quantity of 100 tablets, pharmacist dispensing instructions, and storage details. Manufactured in the Czech Republic. The label features a serialization coding area and the Teva logo.*

FDA Label Image

Label-400mg (Image 9)

Quetiapine Tablets USP 400 mg bottle label by Teva Pharmaceuticals USA Inc. The label includes medication guide instructions, storage information, and a serialization coding area. It indicates a quantity of 100 tablets with Rx only designation, NDC 0093-8165-01, and states the manufacturer is Teva Czech Industries, Czech Republic.*

* 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.