Metoprolol Injection, Solution
Product Images NDC 65219-665

View Photos of 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 (NDC 65219-665). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Metop-img-01.jpg (Metop Img 01)

FDA Label Image

Metop-label-01.jpg (Metop Label 01)

Metop-label-01.jpg (Metop Label 01)
Metoprolol Tartrate Injection USP 5 mg/5 mL (1 mg/mL) single-dose vial label for intravenous use. The label states sterile solution with each 5 mL vial containing 5 mg metoprolol tartrate. It includes storage instructions to keep at 20°C to 25°C, protect from light, and not freeze. Labeler information: Fresenius Kabi USA, LLC, Lake Zurich, IL. Barcode and lot/expiration fields are present.*
FDA Label Image

Metop-label-02.jpg (Metop Label 02)

Metop-label-02.jpg (Metop Label 02)
Label for Metoprolol Tartrate Injection, USP 5 mg/5 mL (1 mg/mL) for intravenous use. The sterile product is supplied as 10 x 5 mL single-dose vials. Storage instructions range from 20°C to 25°C (68°F to 77°F), with USP controlled room temperature noted. The label includes directions to protect from light and to retain in the carton until time of use. The product is labeled by Fresenius Kabi USA, LLC, Lake Zurich, IL, with NDC 65219-665-05.*
FDA Label Image

Metop-struc-01.jpg (Metop Struc 01)

Metop-struc-01.jpg (Metop Struc 01)
Chemical structure depicting the active ingredient Metoprolol Tartrate, showing the molecular arrangement of the metoprolol moiety and the tartrate component.*

* 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.