Metoprolol Tartrate
Product Images NDC 53808-0725

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 53808-0725). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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

Metoprolol Tartrate Structural Formula (8a668014 8811 4b79 91b8 279eb6ea0440 01)

Chemical structure diagram showing two molecules. The left molecule represents the chemical structure consistent with metoprolol tartrate, featuring aromatic and ether groups. The right molecule shows the structure of tartaric acid with hydroxyl and carboxyl groups.*

FDA Label Image

Metoprolol Tartrate Tablets 100 mg Bottles (Metoprolol 100mg(mylan))

Label for Metoprolol Tartrate 100 mg tablets, packaged by DOH Central Pharmacy in Tallahassee, FL. The label shows quantity of 30 tablets, RX only, and includes a barcode with UPC 303780047105.*

FDA Label Image

Metoprolol Tartrate Tablets 25 mg Bottles (Metoprolol 25mg(mylan))

Label for Metoprolol Tartrate 25 mg tablets, quantity 30, prescription only, labeled by State of Florida DOH Central Pharmacy in Tallahassee, FL. The label includes lot number, expiration date, and a UPC barcode.*

FDA Label Image

Metoprolol Tartrate Tablets 50 mg Bottles (Metoprolol 50mg(mylan))

Label for Metoprolol 50 mg tablets, quantity of 30, labeled RX Only. The label includes manufacturer information as Mylan and packaging by DOH Central Pharmacy, Tallahassee, FL. It shows a lot number and expiration date, along with a UPC barcode.*

* 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.