Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 55154-7280

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 55154-7280). 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

E0258f08 1b95 40f0 Be39 B14556f672c4 00

Metoprolol succinate extended-release tablets USP 25 mg film-coated, presented in a 10-tablet unit dose package. The label includes dosage information, storage instructions (20°-25°C), and warnings indicating the package is not child resistant and intended for institutional use. Manufactured by Dr. Reddy's Laboratories Limited and distributed by Major Pharmaceuticals and Cardinal Health.*

FDA Label Image

Figure (Figure)

A forest plot chart titled "Results for Subgroups in MERIT-HF," displaying relative risk and 95% confidence intervals for various clinical subgroups comparing metoprolol succinate extended-release tablets versus placebo. The chart includes three outcome columns: total mortality, total mortality or all-cause hospitalization (time to first event), and total mortality or hospitalization for heart failure (time to first event). Subgroups are listed on the vertical axis, with relative risk on the horizontal axis.*

FDA Label Image

Structure (Structure)

Chemical structure diagram for metoprolol succinate, illustrating the molecular arrangement of the active ingredient in the medication Metoprolol succinate 25 mg extended-release tablets by Cardinal Health 107, 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.