Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 50090-5721

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 50090-5721). 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 (Lbl500905721)

Label Image (Lbl500905721)
Metoprolol Succinate 100 mg extended-release film-coated tablets packaging label from A-S Medication Solutions. The label indicates the product is oral tablets with 90 count and includes storage instructions to keep at 77 degrees Fahrenheit. The NDC number 50090-5721 is displayed along with lot and dosage code information.*
FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Metoprolol-structure (Metoprolol Structure)
Chemical structure diagram of metoprolol succinate, showing the metoprolol molecule linked with succinate components as part of the extended-release formulation.*
FDA Label Image

Metoprolol-table1a (Metoprolol Table1a)

Metoprolol-table1a (Metoprolol Table1a)
A forest plot titled 'Results for Subgroups in MERIT-HF' illustrating relative risk and 95% confidence intervals for Metoprolol Succinate Extended-Release Tablets versus placebo. It includes three outcomes: Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality or Hospitalization for Heart Failure, across various subgroups like US, Non-US, NYHA classifications, ejection fraction, etiology, sex, race, prior myocardial infarction, diabetes status, hypertension status, 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.