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

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 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)

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)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.