Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 55154-4698

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 55154-4698). 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.

FDA Label Image

Bag Label (028049cd D233 49f9 87fa Ec91e433a49f 00)

Metoprolol Succinate Extended-Release Tablets USP 25 mg, film-coated extended-release oral tablets. The label states a count of 10 tablets per package. The labeler is Cardinal Health 107, LLC with product NDC 55154-4698. Additional caution and storage instructions, dosage note, and packaging details are included.*

FDA Label Image

Drr04661

Metoprolol Succinate 25 mg extended-release film-coated tablet, white and oval-shaped. One side is scored and engraved with 'M' and '1,' and the other side is scored without markings. Oral dosage form manufactured by Cardinal Health 107, LLC.*

FDA Label Image

Figure (Figure)

A forest plot presenting subgroup analysis results from the MERIT-HF study. It compares relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups include patient characteristics such as region, NYHA class, ejection fraction, ischemic etiology, sex, race, prior myocardial infarction, diabetes status, hypertension, and heart rate categories.*

FDA Label Image

Structure (Structure)

Chemical structure of Metoprolol Succinate showing the molecular arrangement of its components, including aromatic rings, hydroxyl groups, and succinate moieties.*

* 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.