Metoprolol Succinate Tablet, Extended Release
Product Images NDC 68071-3828

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 68071-3828). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceutcals, 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.

Product Images & Figures Index

FDA Label Image

Pdp (68071 3828 1)

Pdp (68071 3828 1)
Metoprolol succinate 50 mg extended-release tablets package label by NuCare Pharmaceuticals, Inc. The label states each film-coated tablet contains 47.5 mg Metoprolol Succinate equivalent to 50 mg Metoprolol Tartrate, USP. Package contains 100 tablets, Rx only, with storage recommended at controlled temperature 68-77°F. Manufacturer details and barcode are included.*
FDA Label Image

Figure (Figure)

Figure (Figure)
A forest plot 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). The chart compares metoprolol succinate extended-release tablets versus placebo across various subgroups such as geographic region (U.S., Non-U.S.), NYHA class, ejection fraction levels, ischemic and non-ischemic etiology, sex, race, previous myocardial infarction status, diabetes mellitus, hypertension, and heart rate.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Metoprolol succinate, showing the molecular arrangement of metoprolol with two succinate 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.