Metoprolol Succinate Tablet, Extended Release
Product Images NDC 68788-8448

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 68788-8448). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Metoprolol Succinate Extended-release Tab Usp 100mg (0ded3105 B962 4748 Bf5b Fca7a4557562 00)

Label for Metoprolol Succinate Extended-Release Tablets USP 100 mg by Preferred Pharmaceuticals Inc, generic for Toprol XL. The label includes dosage form as oral tablet extended release, a barcode, storage instructions, manufacturer Oryza Pharmaceuticals, and bilingual directions for use in English and Spanish on a yellow background.*

FDA Label Image

Figure (Figure001)

A forest plot titled "Results for Subgroups in MERIT-HE" showing relative risk and 95% confidence intervals for various subgroups across three outcomes: Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality or Hospitalization for Heart Failure. The horizontal axis represents relative risk values from 0 to 2, with markers indicating whether results favor Metoprolol Succinate Extended-Release Tablets or placebo. Subgroups include demographics, clinical characteristics like ejection fraction, ischemic etiology, diabetes status, and heart rate.*

FDA Label Image

Structure (Structure001)

Chemical structure diagram of Metoprolol Succinate, showing the detailed arrangement of its molecular components including hydroxyl, ether, amine groups, and the 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.