Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 55154-4347

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 55154-4347). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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 (Figure)

Figure (Figure)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' illustrating relative risk and 95% confidence intervals for three outcomes: total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The chart compares subgroups favoring metoprolol succinate extended-release tablets versus placebo across various patient categories including U.S. and non-U.S., NYHA classes, ejection fraction ranges, ischemic etiology, sex, race, myocardial infarction history, diabetes status, hypertension status, and heart rate groups.*
FDA Label Image

100mg Bag Label (Image 01)

100mg Bag Label (Image 01)
Label for Metoprolol Succinate extended-release tablets USP, 100 mg strength, in a package containing 10 tablets. The label includes storage instructions, usage warnings, and manufacturer information, specifying Cardinal Health 107, LLC as the labeler, with product NDC 55154-4347.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Metoprolol Succinate, showing the molecular arrangement of its components including aromatic and aliphatic groups, as part of its extended-release tablet formulation.*

* 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.