Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 72789-284

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 72789-284). 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.

Product Images & Figures Index

FDA Label Image

72789284 Label (72789284)

72789284 Label (72789284)
Metoprolol succinate ER 50 mg extended-release film-coated tablets label by PD-Rx Pharmaceuticals, Inc. The label shows a 30-tablet package with NDC 72789-284-30. It includes dosage and storage warnings, expiration date 10/2023, lot number J22E36, and manufacturer information. The label has directions for use space and a barcode with QR code.*
FDA Label Image

Figure (Figure)

Figure (Figure)
A forest plot showing subgroup analysis results from the MERIT-HF study. It compares the 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 patient subgroups such as geographic location, NYHA class, ejection fraction, etiology, sex, race, previous myocardial infarction, diabetes status, hypertension status, and heart rate.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of metoprolol succinate showing the molecular arrangement of metoprolol combined with succinic acid, illustrating the extended release formulation's compound components.*

* 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.