Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 72789-535

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 72789-535). 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

72789535 Label (72789535)

72789535 Label (72789535)
Metoprolol Tartrate USP 50 mg film-coated tablets packaging label by PD-Rx Pharmaceuticals, Inc. The label indicates a package containing 90 tablets with NDC 72789-535-90. It includes dosage strength, expiration date (10/2027), lot number (K25D63), barcode, and warning to keep out of reach of children and dosage/storage instructions to see package insert.*
FDA Label Image

Chemical Structure (Metoprolol Str)

Chemical Structure (Metoprolol Str)
Chemical structure diagram of Metoprolol Tartrate showing its molecular components, including aromatic rings, hydroxyl groups, and the tartrate 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.