Metoprolol Succinate Tablet, Extended Release
Product Images NDC 50090-5418

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 50090-5418). 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 (Fe222a69 B261 4e41 83ab Af76ee17812d 01)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 01)
Chemical structure of metoprolol succinate showing the molecular arrangement of the active ingredient in the medication.*
FDA Label Image

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)
A forest plot presenting results for subgroups in the MERIT-HF study. It compares relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups include various demographic and clinical characteristics such as region, NYHA class, ejection fraction, and comorbidities. The plot indicates whether data favors metoprolol succinate or placebo.*
FDA Label Image

Label Image (Lbl500905418)

Label Image (Lbl500905418)
Metoprolol succinate 25 mg extended-release tablets carton from A-S Medication Solutions. The label indicates metoprolol succinate tablets, 25 mg strength, in a package of 30 extended-release tablets. Storage instructions specify 68 to 77 degrees Fahrenheit. The label includes a barcode and manufacturing information.*

* 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.