Metoprolol Succinate
Product Images NDC 71335-2644

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 71335-2644). 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

Figure (Figure001)

Figure (Figure001)
A forest plot titled 'Results for Subgroups in MERIT-HE' displaying relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The chart compares outcomes favoring Metoprolol Succinate Extended-Release Tablets versus placebo across various subgroups such as US/non-US, NYHA class, ejection fraction levels, ischemic etiology, sex, race, previous myocardial infarction, diabetes mellitus status, hypertension history, and heart rate categories.*
FDA Label Image

Label (Lbl713352644)

Label (Lbl713352644)
Label for Metoprolol Succinate Extended-Release Tablets, USP 200 mg, containing 30 tablets. The label shows the product NDC 71335-2644-1 and indicates the tablets are repackaged by Bryant Ranch Prepack, Inc., and manufactured by Visum Pharmaceutical Co., Ltd. Additional details include storage instructions and a pharmacist advisory link.*
FDA Label Image

Structure (Structure001)

Structure (Structure001)
Chemical structure diagram of Metoprolol Succinate showing the molecular arrangement of its components including aromatic ring, hydroxyl, amine groups, 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.