Seroquel
Product Images NDC 69189-0484

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Seroquel (NDC 69189-0484). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avera Mckennan Hospital, 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 Xr 300 mg Tablet (6918904841)

Quetiapine Xr 300 mg Tablet (6918904841)
This is a medication information which includes the name, strength, and manufacturer details of two drugs, QUET|APINE XR 310 MG and SEROQUEL XR 300 MG TABLET manufactured by AstraZeneca. Additionally, it also provides other details such as the manufacturing and hospital lot numbers, expiration date, and the National Drug Code (NDC) for one of the drugs. The location of the hospital where the drug is possibly being used is also mentioned, which is Avera McKennan in Sioux Falls.*
FDA Label Image

Structural Formula (Image 01)

FDA Label Image

Figure 1 Kaplan-meier Curves Of Time To Schizophrenic Relapse Study 3.jpg (Image 02)

FDA Label Image

Figure 2 Kaplan-maier Curves Of Time To Recurrence Of A Mood Event.jpg (Image 03)

FDA Label Image

Figure 3 Kaplan-meier Curves Of Time To Recurrence Of A Mood Event (study 19).jpg (Image 04)

Figure 3 Kaplan-meier Curves Of Time To Recurrence Of A Mood Event (study 19).jpg (Image 04)
The text indicates a chart or graph displaying the proportion of patients with relapse over time in weeks. The chart shows two different rates or treatments, labeled "VAL" and "PLac LwAL". However, without more context or a title, it is unclear what type of patients or condition is being measured.*

* 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.