Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 55154-6886

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 55154-6886). 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

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Label for Metoprolol succinate extended-release tablets USP 50 mg, film-coated, 10 tablets per package. The label states the active ingredient strength, storage instructions (20°-25°C), and that it is RX only. Manufactured by Dr. Reddy's Laboratories Ltd, India, and distributed by Major Pharmaceuticals, MI and Cardinal Health, OH, USA. Includes a barcode and NDC 55154-6886-0.*
FDA Label Image

Figure

Figure
A forest plot titled 'Results for Subgroups in MERIT-HF' showing the relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure across various patient subgroups. The subgroups are listed on the vertical axis and include clinical and demographic factors. Each plot compares metoprolol succinate extended-release tablets to placebo, with risk indicators and confidence intervals displayed for each subgroup.*
FDA Label Image

Structure

Structure
Chemical structure of Metoprolol succinate showing its molecular arrangement including aromatic ring, hydroxyl groups, and 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.