Metoprolol Succinate Tablet, Extended Release
Product Images NDC 50090-6448

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-6448). 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

Figure (Figure001)

A forest plot chart titled 'Results for Subgroups in MERIT-HE' showing relative risk and 95% confidence intervals for various subgroups related to total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The chart compares effects favoring Metoprolol Succinate extended-release tablets versus placebo for subgroups such as geographic location, NYHA class, ejection fraction, etiology, sex, race, myocardial infarction history, diabetes mellitus, hypertension, and heart rate.*

FDA Label Image

Label Image (Lbl500906448)

Label for Metoprolol Succinate extended release tablets, 50 mg strength, oral route. The label shows the product NDC 50090-6448, lot number 5954-0, and states a package size of 30 tablets. It is labeled by A-S Medication Solutions in Libertyville, Illinois, and includes storage instructions to protect from moisture and store at 77 degrees Fahrenheit.*

FDA Label Image

Structure (Structure001)

Chemical structure of the active ingredient Metoprolol Succinate, showing its molecular arrangement including aromatic ring, 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.