Metoprolol Succinate Tablet, Extended Release
Product Images NDC 71335-1951

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 71335-1951). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 diagram of metoprolol succinate, showing the molecular components and arrangement characteristic of this active ingredient.*
FDA Label Image

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for outcomes including Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality or Hospitalization for Heart Failure. The plot compares risks for metoprolol succinate versus placebo across subgroups such as region (US, Non-US), NYHA class, ejection fraction levels, ischemic etiology, sex, race, previous myocardial infarction, diabetes status, hypertension history, and heart rate categories.*
FDA Label Image

Label (Lbl713351951)

Label (Lbl713351951)
Metoprolol Succinate ER 100 mg extended-release tablets packaged by Bryant Ranch Prepack. The label compares the product to Toprol XL 100 mg tablets by Cadila Healthcare Limited. It includes storage instructions to keep tightly closed and store at 20°-25°C (68°-77°F). The package size is 30 tablets with NDC 71335-1951.*

* 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.