Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 50090-7591

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-7591). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 Image (Lbl500907591)

Metoprolol Succinate 25 mg extended-release film-coated tablets label from A-S Medication Solutions. The label includes dosage information, lot number, storage instructions at 77 degrees Fahrenheit, and package size of 90 tablets. The medication is for oral use and labeled with NDC 50090-7591.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart titled 'Results for Subgroups in MERIT-HF,' showing relative risk and 95% confidence intervals for various subgroups. The chart compares effects of metoprolol succinate extended-release tablets versus placebo on total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure across different patient groups. Subgroups include geographic regions, NYHA classification, ejection fraction, ischemic etiology, sex, race, myocardial infarction history, diabetes status, hypertension history, and heart rate categories.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure of metoprolol succinate, showing the molecular arrangement including phenyl and succinate groups.*

* 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.