Metoprolol Succinate Tablet, Extended Release
Product Images NDC 82804-198

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 82804-198). 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

Figure (0d89802b 2784 4eeb 977c 299ab20fd53e 01)

Chemical structure of metoprolol succinate, showing the molecular arrangement of the active ingredient in the medication.*

FDA Label Image

Figure (0d89802b 2784 4eeb 977c 299ab20fd53e 02)

A forest plot chart titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for metoprolol succinate compared to placebo across subgroups. The plot has three panels depicting Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality or Hospitalization for Heart Failure. Subgroups include geographic region, NYHA class, ejection fraction, ischemic etiology, sex, race, previous myocardial infarction, diabetes status, hypertension status, and heart rate. The x-axes represent relative risk favoring either metoprolol succinate or placebo.*

FDA Label Image

82804-198-90 (Image 01)

Label for Metoprolol Succinate 50 mg extended-release tablets by Proficient Rx LP. The label states each film-coated tablet contains metoprolol succinate equivalent to 50 mg metoprolol tartrate. Tablets are described as white to off-white, round, biconvex, debossed with '565' on one side and a break line on the other. Manufacturer is Zydus Lifesciences Ltd., Ahmedabad, India. Storage instructions and multiple small labels with lot and expiration placeholders are also visible.*

* 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.