Metoprolol Tartrate Injection, Solution
Product Images NDC 0409-1778

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 Tartrate (NDC 0409-1778). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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 01)

FDA Label Image

Logo (Metoprolol 02)

FDA Label Image

Principal Display Panel (5 mL Vial Label)

Principal Display Panel (5 mL Vial Label)
This is a description of a medication called Metoprolol Tartrate Injection, USP. It is contained in a single-dose vial and is for intravenous use only, and should be protected from light. The product is distributed by Hospira, Inc in Lake Forest, USA. It is stored at 20 to 25°C (68 to 77°F). The product is labeled with the lot number, expiration date and NDC code.*
FDA Label Image

Principal Display Panel (5 mL Vial Carton)

Principal Display Panel (5 mL Vial Carton)
This is a package of 10 single-dose fliptop vials of Metoprolol Tartrate Injection, USP with each vial containing 5 mg/5 mL (1 mg/mL). The vial should be stored at a controlled room temperature between 20 to 25°C. It is for intravenous use and must be protected from light. The content of each L container is 5 mg Metoprolol Tartrate and 45 mg Sodium Chloride USP in Water for Injection USP. This product is distributed by Hospira, Inc.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.