Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 72789-576

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 72789-576). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

Image (72789576)

Packaging label for Metoprolol Succinate extended-release tablets USP, 25 mg strength, supplied in a bottle of 90 tablets. The product is marked Rx only and is marketed and packaged by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK, with manufacturing by Granules India Limited, Hyderabad, India. The label includes dosage form, storage instructions, barcode, and various regulatory codes.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

A forest plot chart titled 'Results for Subgroups in MERIT-HF' showing the relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The chart compares outcomes favoring metoprolol succinate extended-release tablets versus placebo across subgroups including U.S., non-U.S., NYHA classes I-IV, ejection fraction categories, ischemic etiology, sex, race, myocardial infarction history, diabetes status, hypertension status, and heart rate groups.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure diagram of metoprolol succinate, showing the molecular arrangement of the active ingredient including the aromatic ring, side chains, and succinate moiety.*

* 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.