Metoprolol Succinate Tablet, Extended Release
Product Images NDC 82868-083

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 82868-083). 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.

Product Images & Figures Index

FDA Label Image

Figure (0d89802b 2784 4eeb 977c 299ab20fd53e 01)

Figure (0d89802b 2784 4eeb 977c 299ab20fd53e 01)
Chemical structure of metoprolol succinate, showing the molecular arrangement of the active ingredient metoprolol succinate.*
FDA Label Image

Figure (0d89802b 2784 4eeb 977c 299ab20fd53e 02)

Figure (0d89802b 2784 4eeb 977c 299ab20fd53e 02)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for metoprolol succinate versus placebo. The chart includes subgroup categories such as region, NYHA class, ejection fraction, etiology, sex, race, medical history, and heart rate. Three outcomes are compared: total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure.*
FDA Label Image

Label (82868 083 30 Rev A 06 25 Nhc)

Label (82868 083 30 Rev A 06 25 Nhc)
Label for metoprolol succinate extended-release tablets, USP, 25 mg strength, containing 30 tablets. The label indicates prescription only and storage instructions at controlled room temperature. It also includes repackaging and manufacturer information for Northwind Health Company, LLC.*

* 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.