Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 70518-3291

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 70518-3291). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Metoprolol Tartrate is prescription-only medication manufactured by Rising Pharma, Inc., Allendale, NJ. The National Drug Code (NDC) for this medication is 70518-3291-00, and the Source NDC is 57237-0100-99. The LOT number and expiration date are not available. The patient should keep this medication out of reach of children. The medication should be stored in a cool and dry place. The directions of use are provided in the package insert. The medication is repackaged by RemedyRepack Inc., Indiana, PA.*

FDA Label Image

Metoprolol-structure (Metoprolol Str)

* 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.