Levophed Injection, Solution, Concentrate
Product Images NDC 0409-0161

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 Levophed (NDC 0409-0161). 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 (Levophed 01)

Chemical Structure (Levophed 01)
Chemical structure diagram of norepinephrine bitartrate, showing the molecular arrangement of the norepinephrine component and the bitartrate moiety with a water molecule (H2O).*
FDA Label Image

Logo (Levophed 02)

FDA Label Image

Principal Display Panel (4 mL Vial Label)

Principal Display Panel (4 mL Vial Label)
Label for LEVOPHED injection, USP 4 mg/4 mL (1 mg/mL) concentrate for intravenous infusion. The label shows the proprietary name Levophed and the generic name norepinephrine bitartrate. It states a 4 mL fill in a 5 mL single-dose fliptop vial. Distributed by Hospira, Inc., Lake Forest, IL. Includes barcodes and space for lot and expiration dates.*
FDA Label Image

Principal Display Panel (4 mL Vial Carton)

Principal Display Panel (4 mL Vial Carton)
Packaging label for Levophed 4 mg/4 mL (1 mg/mL) norepinephrine bitartrate injection, USP, injectable concentrate for intravenous use. The label indicates a 4 mL volume per vial, with a total of 10 single-dose fliptop vials per package. The labeler is Hospira, Inc., and the NDC is 0409-0161-10. Warnings include dosage control, avoiding extravasation, and protection from light.*

* 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.