Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 71610-138

4 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 71610-138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Bottle Label 25 mg (71610 0137 60)

Bottle Label 25 mg (71610 0137 60)
Label for Metoprolol Tartrate 25 mg tablets, film-coated, oral administration. The package contains 90 tablets. Manufactured by AuroLife Pharma, LLC, Dayton, NJ, and repackaged by Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN. Label indicates storage instructions and RX only status.*
FDA Label Image

Bottle Label 50 mg (71610 0138 60)

Bottle Label 50 mg (71610 0138 60)
Label for Metoprolol Tartrate 50 mg film-coated tablets, containing 90 tablets. The label specifies storage instructions between 68-77 degrees Fahrenheit and indicates the product is repackaged by Aphena Pharma Solutions - Tennessee, LLC. It includes barcodes and mentions prescription use only (RX Only).*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Metoprolol-structure (Metoprolol Str)

Metoprolol-structure (Metoprolol Str)
Chemical structure of Metoprolol Tartrate showing the molecular arrangement of its components, including the metoprolol moiety and tartaric acid part.*

* 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.