Metoprolol Succinate Tablet, Extended Release
Product Images NDC 70518-4090

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 70518-4090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Metoprolol Succinate 25 mg extended-release oral tablets packaging label from RemedyRepack Inc. The label indicates a quantity of 5 tablets and includes storage instructions to protect from moisture and keep out of reach of children. It displays the NDC number 70518-4090-00 and manufacturer information for Oryza Pharmaceuticals Inc.*
FDA Label Image

Figure (Figure001)

Figure (Figure001)
A forest plot depicting the results for subgroups in the MERIT-HE study. The chart shows relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization (time to first event), and total mortality or hospitalization for heart failure (time to first event). Data are stratified by demographic and clinical subgroups including geographic location, NYHA class, ejection fraction, ischemic etiology, sex, race, prior myocardial infarction, diabetes status, hypertension history, and heart rate.*
FDA Label Image

Structure (Structure001)

Structure (Structure001)
Chemical structure of Metoprolol Succinate, depicting its molecular arrangement with hydroxyl groups, methoxy groups attached to a benzene ring, and succinate 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.