Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 82804-279

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 82804-279). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

82804-279-90 (Image 01)

Label for Metoprolol Succinate 100 mg extended-release oral tablets by Proficient Rx LP. The label shows 90 tablets, with product ID ZM027990. Tablets are described as white to off-white, round, film-coated, scored with debossed markings. Manufacturer listed as Granules India Limited, Hyderabad, India. Storage instructions included.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart showing results for subgroups in the MERIT-HF study. It compares relative risk and 95% confidence intervals for outcomes including total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, favoring metoprolol succinate extended-release tablets versus placebo across different subpopulations such as U.S. vs. non-U.S., NYHA classes, ejection fraction levels, ischemic etiology, sex, race, myocardial infarction history, diabetes status, hypertension history, and heart rate groups.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure of metoprolol succinate, showing the molecular arrangement including aromatic rings, hydroxyl groups, ether linkages, 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.