Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 53401-010

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 53401-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Label (53401 0010 30)

Metoprolol Succinate ER, USP 25 mg extended-release film-coated tablets bottle label containing 30 tablets. The label includes storage instructions, manufacturer Dr. Reddy's Laboratories in Princeton, NJ, and repackager Aphena Pharma Solutions, Cookeville, TN. The label shows the NDC number 53401-010-30 and barcodes, with space for lot number, expiration date, and Rx only designation.*

FDA Label Image

Aphena (Aphena)

FDA Label Image

Figure (Figure)

A forest plot chart titled "Results for Subgroups in MERIT-HF" displaying the relative risk and 95% confidence intervals for various subgroups regarding total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The horizontal axis measures relative risk from 0 to 2. Subgroups include geography, heart failure classification, ejection fraction, etiology, sex, race, history of myocardial infarction, diabetes, hypertension, and heart rate. The chart compares favorability between metoprolol succinate extended-release tablets and placebo.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of Metoprolol succinate showing the molecular arrangement of metoprolol linked to succinic acid components.*

* 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.