Metoprolol Succinate Tablet, Extended Release
Product Images NDC 72789-010

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 72789-010). 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

72789010 Label (72789010)

72789010 Label (72789010)
Metoprolol Succinate ER 50 mg extended-release tablets packaging label from PD-Rx Pharmaceuticals, Inc. The label displays the product name, strength, quantity (30 tablets), and NDC number 72789-010-30. It includes warnings about not abruptly stopping the medication, not crushing or chewing, and a highlighted safety warning to keep out of reach of children. Additional details include reorder number, lot number F20A55, and expiration date 10/2021.*
FDA Label Image

Image-01 (Image 01)

Image-01 (Image 01)
Chemical structure diagram showing the molecular formula of metoprolol succinate, including the two succinate moieties depicted on the right side of the image.*
FDA Label Image

Image-02 (Image 02)

Image-02 (Image 02)
A forest plot illustrating results for subgroups in the MERIT-HF study. It presents relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure comparing Metoprolol Succinate extended-release tablets versus placebo across various patient subgroups.*

* 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.