Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-2592

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-2592). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label (Lbl713352592)

This label is for Metoprolol Succinate Extended-Release Tablets, USP, 25 mg, from Bryant Ranch Prepack. The package contains 100 film-coated extended-release tablets. The label includes storage instructions, a warning to keep out of reach of children, and mentions the product is repackaged by Bryant Ranch Prepack and manufactured by Granules India Limited. It features two QR codes and barcodes with NDC 71335-2592-1.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart titled 'Results for Subgroups in MERIT-HF' displaying relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups include geographic location, NYHA class, ejection fraction, ischemic etiology, sex, race, myocardial infarction history, diabetes, hypertension, and heart rate categories. The chart compares outcomes between metoprolol succinate extended-release tablets and placebo.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure diagram of Metoprolol Succinate showing the molecular structure including aromatic ring, hydroxyl group, and succinate moiety with detailed bonds and atom 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.