Linezolid Injection, Solution
Product Images NDC 0409-4883

5 FDA label images from Hospira, Inc. · 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 Linezolid (NDC 0409-4883). 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 (Linezolid 01)

Chemical Structure (Linezolid 01)
Chemical structure of the active ingredient Linezolid. The diagram shows the molecular structure with rings and functional groups typical of Linezolid as an injection solution.*
FDA Label Image

Figure 1 (Linezolid 02)

Figure 1 (Linezolid 02)
A line graph depicting plasma concentration of Linezolid in micrograms per milliliter (µg/mL) over 12 hours after a 600 mg oral dose every 12 hours. The y-axis shows Linezolid plasma concentration, and the x-axis represents time in hours post-dose, including error bars for variability at each time point.*
FDA Label Image

Logo (Linezolid 03)

FDA Label Image

Principal Display Panel (300 mL Bag Label)

Principal Display Panel (300 mL Bag Label)
Linezolid Injection in 0.9% Sodium Chloride 600 mg/300 mL (2 mg/mL) intravenous solution label by Hospira, Inc. The label includes active ingredient content, pH adjustment information, storage instructions, and manufacturer details, with NDC 0409-4883-11 and volume of 300 mL.*
FDA Label Image

Linezolid 05

Linezolid 05
Label for Linezolid Injection in 0.9% Sodium Chloride, 600 mg/300 mL (2 mg/mL) intravenous infusion solution. The single-dose container label shows the product name, strength, volume (300 mL), route (intravenous), NDC 0409-4883-11, and Hospira, Inc. as the labeler. Instructions include tearing at notch to open and caution about single-use and proper storage.*

* 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.