Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 51655-281

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 Tartrate (NDC 51655-281). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 281 25 Master Bottle Label Approval Rev A 05 22)

Label (51655 281 25 Master Bottle Label Approval   Rev A 05 22)
Label for Metoprolol Tartrate 50 mg film-coated tablets, USP, containing 60 tablets. The label includes storage instructions at 20°-25°C and warnings to keep out of reach of children, store in the original container, protect from moisture, and keep the container tightly closed. Manufactured by Northwind Pharmaceuticals, distributed by Northwind Health Company, LLC.*
FDA Label Image

Metoprolol Tartrate Tabs Usp 50mg Image

Metoprolol Tartrate Tabs Usp 50mg Image
Metoprolol Tartrate 50 mg film-coated tablet, round and pink, imprinted with 'R 50'. This oral tablet is a prescription drug labeled by Northwind Health Company, LLC.*
FDA Label Image

Chemical Structure (Metoprolol Tartrate Tabs Usp Structure)

Chemical Structure (Metoprolol Tartrate Tabs Usp Structure)
Chemical structure of Metoprolol Tartrate, showing the molecular arrangement of its components including the metoprolol moiety and tartaric acid portion.*

* 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.