Metoprolol Tartrate Injection, Solution
Product Images NDC 72572-420

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 72572-420). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Chemical Structure (Metoprolol Tartrate Injection Usp Civica 1)

Chemical structure diagram showing the molecular structure of Metoprolol Tartrate, the active ingredient in the injection solution product.*

FDA Label Image

Label (Metoprolol Tartrate Injection Usp Civica 2)

Metoprolol Tartrate Injection, USP 5 mg/5 mL (1 mg/mL) single-dose vial label. The injection solution is for intravenous use only, supplied by Civica Inc. The label includes storage instructions, dosing guidance, manufacturer details, and a barcode with lot and expiration date fields.*

FDA Label Image

Shelfpack (Metoprolol Tartrate Injection Usp Civica 3)

Label for Metoprolol Tartrate Injection, USP 5 mg per 5 mL (1 mg/mL) intravenous solution. The label includes dosage strength, usage instructions for IV use only, packaging size of 10 single-dose 5 mL vials, and manufacturer information including Civica, Inc. and Hikma Farmacêutica (Portugal). Storage instructions and barcode are also visible.*

FDA Label Image

Layout 1 (Metoprolol Tartrate Injection Usp Civica 4)

Packaging label for Metoprolol Tartrate injection, solution, 5 mg/5 mL, for intravenous use. The label includes a GTIN barcode, serial number, expiration date placeholder, and lot number. The labeler is Civica, Inc. The product NDC is 72572-420.*

* 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.