Metoprolol Succinate Tablet, Extended Release
Product Images NDC 50090-6489

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-6489). 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

Figure (Figure001)

A forest plot chart titled "Results for Subgroups in MERIT-HE" showing relative risk and 95% confidence intervals for subgroups comparing Metoprolol Succinate Extended-Release Tablets versus placebo. It covers three outcomes: Total Mortality, Total Mortality or All-Cause Hospitalization (Time to First Event), and Total Mortality or Hospitalization for Heart Failure (Time to First Event), across various subgroups such as geographic region, NYHA class, ejection fraction, ischemic etiology, sex, race, history of MI, diabetes status, hypertension, and heart rate.*

FDA Label Image

Label Image (Lbl500906489)

Metoprolol Succinate 25 mg extended release oral tablets, packaged by A-S Medication Solutions. The label shows a bottle containing 90 tablets, with instructions to store at room temperature and protect from moisture. The NDC is 50090-6489-0 and the product number is 9510-0.*

FDA Label Image

Structure (Structure001)

Chemical structure of Metoprolol Succinate showing its detailed molecular formula, including a benzene ring, various oxygen, nitrogen, and carbon atoms arranged with hydroxyl and methoxy groups.*

* 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.