Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-3052

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-3052). 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 (Lbl713353052)

Label for Metoprolol Succinate Extended-Release Tablets USP, 50 mg strength, film-coated oral tablets. The label indicates a package count of 30 tablets. It is repackaged by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Granules India Limited. The NDC number is 71335-3052-1. Includes storage instructions and QR codes for additional prescribing information.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart titled 'Results for Subgroups in MERIT-HF' comparing the relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure between metoprolol succinate extended-release tablets and placebo. The chart includes subgroups based on geography, NYHA class, ejection fraction, ischemic etiology, sex, race, myocardial infarction history, diabetes, hypertension, and heart rate.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure diagram showing the molecular formula of Metoprolol Succinate, the active ingredient in Metoprolol Succinate 50 mg extended-release tablets. The structure includes detailed chemical bonds and groups characteristic of Metoprolol Succinate salt composition.*

* 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.