Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-2811

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-2811). 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 (Lbl713352811)

Label for Metoprolol Succinate Extended-Release Tablets, USP, 200 mg strength. The label indicates a package size of 30 tablets, repackaged by Bryant Ranch Prepack, Inc. in Burbank, CA, and manufactured by Granules India Limited. The label also includes storage instructions and dosage information references, with the product NDC 71335-2811.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart titled "Results for Subgroups in MERIT-HF" showing relative risk and 95% confidence intervals for various subgroups including geographic location (U.S., Non-U.S.), NYHA classes, ejection fraction levels, ischemic etiology, sex, race, MI history, diabetes status, hypertension history, and heart rate categories. The chart compares outcomes for metoprolol succinate extended-release tablets versus placebo across three endpoints: total mortality; total mortality or all-cause hospitalization; and total mortality or hospitalization for heart failure.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure diagram showing the molecular structure of Metoprolol Succinate, an active ingredient in film-coated extended-release tablets.*

* 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.