Metoprolol Injection
Product Images NDC 83270-177

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol (NDC 83270-177). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oneosource Specialty Pharma Limited, 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

Carton-label-5ml (5 mg Per 5 mL Carton Label)

Carton-label-5ml (5 mg Per 5 mL Carton Label)
Package label for Metoprolol Tartrate Injection, USP 5 mg per 5 mL intravenous injection by Oneosource Specialty Pharma Limited. It contains 10 single-dose vials of 5 mL each, with 1 mg/mL concentration. The label includes storage instructions, manufacturer details, and a barcode.*
FDA Label Image

Vial-label-5ml (5 mg Per 5 mL Vial Label)

Vial-label-5ml (5 mg Per 5 mL Vial Label)
Label for Metoprolol Tartrate Injection, USP 5 mg per 5 mL (1 mg/mL) intravenous single-dose vial. The label includes storage instructions (20° to 25°C), formulation details, and manufacturer information for OneSource Specialty Pharma Limited, Bangalore, India. The vial is sterile, latex-free, nonpyrogenic, and preservative-free.*
FDA Label Image

Metoprolol-structure (Metoprolol Tartrate Structure)

Metoprolol-structure (Metoprolol Tartrate Structure)
Chemical structure diagram showing the molecular structure of Metoprolol Tartrate, including two main components linked together, one being the metoprolol molecule and the other the tartaric acid molecule.*

* 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.