Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 51655-534

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 51655-534). 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 534 25 Master Bottle Label Approval Rev A 02 22)

Label (51655 534 25 Master Bottle Label Approval   Rev A 02 22)
Label for Metoprolol Tartrate Tablets USP 25 mg, film-coated oral tablets. The package contains 60 tablets and is labeled Rx only. Storage instructions specify 20°-25°C with excursions permitted to 15°-30°C. The label lists the manufacturer as Northwind Pharmaceuticals and includes batch and expiration information.*
FDA Label Image

Metoprolol-structure (Metoprolol Str)

Metoprolol-structure (Metoprolol Str)
Chemical structure of Metoprolol Tartrate depicting its molecular components and the tartrate salt.*

* 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.