Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 72789-549

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 72789-549). 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

72789549 Label (72789549)

72789549 Label (72789549)
The label for Metoprolol Tartrate 50 mg film-coated tablets indicates it is an oral prescription medication. The package contains 180 tablets, marketed and packaged by PD-Rx Pharmaceuticals, Inc., and distributed by Rising Pharma Holdings, Inc. The label includes dosage instructions, storage information, and warnings about child safety. It also shows a barcode, QR codes, and expiration date of 05/2025.*
FDA Label Image

Chemical Structure (Metoprolol Str)

Chemical Structure (Metoprolol Str)
Chemical structure of Metoprolol Tartrate showing the molecular connectivity and arrangement of functional groups, including hydroxyl, ether, and carboxyl groups, depicted with standard chemical notation for the active pharmaceutical ingredient.*

* 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.