Metoprolol Succinate Tablet, Extended Release
Product Images NDC 50090-7070

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 50090-7070). 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.

Product Images & Figures Index

FDA Label Image

Figure (Figure)

Figure (Figure)
A forest plot chart titled "Results for Subgroups in MERIT-HF" showing relative risk and 95% confidence intervals for three outcomes: total mortality, total mortality or all-cause hospitalization (time to first event), and total mortality or hospitalization for heart failure (time to first event). Subgroups include geographical region, NYHA class, ejection fraction levels, ischemic etiology, sex, race, presence of previous myocardial infarction, diabetes mellitus, hypertension, and heart rate categories. The chart compares favoring metoprolol succinate extended-release tablets versus placebo across these subgroups.*
FDA Label Image

Label Image (Lbl500907070)

Label Image (Lbl500907070)
Metoprolol succinate extended-release tablets, 100 mg, from A-S Medication Solutions. The label indicates the product is oral, includes a lot number and storage instructions to keep at 68 to 77 degrees Fahrenheit. It states there are 90 tablets in the package and provides the product NDC 50090-7070.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of metoprolol succinate showing the molecular arrangement of metoprolol and succinate components as presented in the image.*

* 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.