Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 82804-262

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 82804-262). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

82804-262-90 (Image 01)

Label for Metoprolol Succinate 25 mg extended-release tablets by Proficient Rx LP. The label includes the NDC 82804-262-90 and states each tablet contains 23.75 mg metoprolol succinate USP equivalent to 25 mg metoprolol tartrate USP. Describes tablets as white to off-white, oval, film coated with debossed scores. Manufactured by Granules India Limited, Hyderabad, India. Storage instruction: 20°-25°C.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot showing results for subgroups in the MERIT-HF study. It compares relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, between metoprolol succinate extended-release tablets and placebo across various subgroups such as geographic region, NYHA class, ejection fraction, ischemic etiology, sex, race, medical history, diabetes status, hypertension, and heart rate.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure diagram of metoprolol succinate, showing the molecular arrangement of the active ingredient including its aromatic ring and 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.