Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 82868-079

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 82868-079). 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 079 30 Rev A 09 25 Nhc)

Label for Metoprolol Succinate extended-release film-coated tablets, USP 100 mg strength. The package contains 30 oral tablets, Rx only. Labeler is Northwind Health Company, LLC. Storage instructions and warnings to keep out of reach of children are included. NDC code 82868-079-30 is shown.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart titled 'Results for Subgroups in MERIT-HF' displaying relative risk and 95% confidence intervals for various subgroups comparing metoprolol succinate extended-release tablets versus placebo. The chart includes three measures: total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups analyzed include geographic regions, NYHA classifications, 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 of its components with two main parts including the aromatic ring 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.