Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 50090-5720

3 FDA label images from A-s Medication Solutions · 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 50090-5720). 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 (Lbl500905720)

Label Image (Lbl500905720)
Metoprolol Succinate 100 mg extended-release film-coated tablets label from A-S Medication Solutions. The label indicates each tablet contains 100 mg metoprolol succinate equivalent to 100 mg metoprolol tartrate USP. Package includes 30 tablets with instructions to store at 77 degrees Fahrenheit. Located in Libertyville, Illinois.*
FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Metoprolol-structure (Metoprolol Structure)
Chemical structure diagram of Metoprolol Succinate, showing the molecular arrangement of its components as part of the active ingredient structure.*
FDA Label Image

Metoprolol-table1 (Metoprolol Table1)

Metoprolol-table1 (Metoprolol Table1)
A forest plot showing results for subgroups in the MERIT-HE study, comparing the effects of TOPROL-XL versus placebo on total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. It includes subgroups like geographic region, NYHA class, ejection fraction, etiology, sex, race, prior myocardial infarction, diabetes status, hypertension status, and heart rate, with relative risk and 95% confidence intervals represented on the x-axis.*

* 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.