Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 53401-009

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 53401-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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 (53401 0009 30)

Metoprolol succinate ER USP 50 mg extended-release oral tablets in a package of 30. The label includes storage instructions, manufacturer Dr. Reddy's Laboratories, and repackager Aphena Pharma Solutions - Tennessee, LLC. The NDC listed is 53401-009-30. Additional batch and expiration date fields are present but not filled in.*

FDA Label Image

Aphena (Aphena)

FDA Label Image

Figure (Figure)

A forest plot titled 'Results for Subgroups in MERIT-HF' displaying relative risk and 95% confidence intervals for three categories: Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality or Hospitalization for Heart Failure. Multiple subgroups are listed including geographical region, NYHA class, ejection fraction, etiology, sex, race, prior myocardial infarction, diabetes status, hypertension status, and heart rate. Each subgroup shows comparative risk favoring metoprolol succinate extended-release tablets or placebo.*

FDA Label Image

Structure (Structure)

Chemical structure diagram showing the molecular composition of metoprolol succinate, the active ingredient. The diagram includes structural formulas representing the metoprolol moiety linked to succinate, indicating the molecular connectivity and functional groups.*

* 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.