Metoprolol Succinate Tablet, Extended Release
Product Images NDC 68071-3965

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 68071-3965). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals, Inc., 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

Pdp (68071 3965 9 (2))

Metoprolol Succinate 50 mg extended-release tablets packaging label from NuCare Pharmaceuticals, Inc. The label indicates 90 tablets per container, with product number P1901090. It includes dosing instructions placeholders and warnings to keep out of reach of children and store at controlled temperature 68-77°F. The label also lists manufacturer Visun Pharmaceutical Co., Ltd., Haikou, China.*

FDA Label Image

Figure (Figure001)

A forest plot chart titled 'Results for Subgroups in MERIT-HE' showing relative risk and 95% confidence intervals for Metoprolol Succinate Extended-Release Tablets versus placebo across various subgroups. The chart presents three outcome categories: 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 geography, NYHA class, ejection fraction, etiology, sex, race, myocardial infarction history, diabetes status, hypertension history, and heart rate.*

FDA Label Image

Structure (Structure001)

Chemical structure diagram of Metoprolol Succinate, showing its molecular components including phenyl groups, alcohol, amine, and succinate groups, represented in a two-part formula.*

* 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.