Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 82868-087

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 82868-087). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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 (82868 087 90 Rev A 09 25 Nhc)

Label for Metoprolol Succinate Extended-Release Tablets, USP 25 mg, in a 90-tablet bottle. The label indicates prescription use only, storage instructions, and manufacturing details by Northwind Health Company, LLC. It also lists tablet composition and packaging information with an NDC of 82868-087-90.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for various subgroups comparing metoprolol succinate extended-release tablets versus placebo. The outcomes measured include total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, displayed on a horizontal scale from 0 to 2, with subgroup categories listed vertically on the left.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure diagram depicting the active ingredient Metoprolol Succinate. The structure shows molecular components, including aromatic rings, hydroxyl groups, and succinate moieties, consistent with the extended-release formulation of Metoprolol Succinate.*

* 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.