Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 50090-5723

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-5723). 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 (Lbl500905723)

Label Image (Lbl500905723)
Metoprolol Succinate extended-release film-coated tablets, 50 mg strength, labeled for oral use. The white label includes the product and lot numbers, packaging information stating 90 tablets per package, and storage instructions to keep at 77 degrees Fahrenheit. The labeler is A-S Medication Solutions located in Libertyville, Illinois.*
FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Metoprolol-structure (Metoprolol Structure)
Chemical structure of Metoprolol Succinate shown as the molecular formula with aromatic rings and functional groups, illustrating the detailed arrangement of atoms in this active ingredient.*
FDA Label Image

Metoprolol-table1a (Metoprolol Table1a)

Metoprolol-table1a (Metoprolol Table1a)
A forest plot chart showing subgroup results for Metoprolol Succinate Extended-Release Tablets in the MERIT-HF study. The chart compares total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, with relative risk and 95% confidence intervals across patient subgroups such as region, NYHA class, ejection fraction, etiology, sex, race, history of myocardial infarction and hypertension, and heart rate.*

* 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.