Metoprolol Tartrate Injection, Solution
Product Images NDC 51662-1365

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 51662-1365). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

How Supplied (How Supplied)

How Supplied (How Supplied)
This text provides information about a pharmaceutical product including the product's NDC (National Drug Code), strength (5 mg/5 mL or 1 mg/mL), and package size (5 mL vial in groups of ten).*
FDA Label Image
FDA Label Image

Serialized Labeling (Serialized Labeling)

Serialized Labeling (Serialized Labeling)
This is the information for Metoprolol Tartrate Injection, a medicine that comes in a 5mL vial and is used for intravenous use only. The National Drug Code is 63323-660-05 and it has 5mg/5mL (1mg/mL) strength. The manufacturing package insert should be consulted before use, and HF Acquisition Co. in Mukilteo, WA is responsible for its distribution.*
FDA Label Image

Structure (Structure)

FDA Label Image

Vial Labeling (Vial Labeling)

Vial Labeling (Vial Labeling)
This is a medication called Metoprolol Tartrate, which is available in a 5mg/5mL strength for injection use only. The drug is contained in a single-use vial of 5mL capacity and is administered intravenously. The vial has a prescription-only label, and its NDC number is 63323-660-05.*

* 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.