Linezolid Injection, Solution
Product Images NDC 0409-4883

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 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)

FDA Label Image

Figure 1 (Linezolid 02)

Figure 1 (Linezolid 02)
This is a graph showing Linezolid plasma concentrations in pg/mL over time after administering 600mg orally every 12 hours. There are measurements taken up to 12 hours after the dose.*
FDA Label Image

Logo (Linezolid 03)

FDA Label Image

Principal Display Panel (300 mL Bag Label)

Principal Display Panel (300 mL Bag Label)
This is a 300mL single-dose container of Linezolid Injection in 0.9% sodium chloride with a concentration of 600mg/300mL (2mg/mL) for intravenous infusion. Each mL contains Linezolid, citric acid anhydrous, sodium hydroxide, and sodium chloride. It is sterile and non-pyrogenic and must be stored at 20 to 25°C. It is a trademark of Hospira available by prescription only. If the text is for anything else other than this medication, it is not-available.*
FDA Label Image

Linezolid 05

Linezolid 05
Linezolid Injection in 0.9% Sodium Chloride is a single-dose container with 2mg and 1.82mg of Linszold and G Acid Anhydrous USP, respectively, that is used for intravenous infusion. It also contains Sodium Hydioside and Sodium Clorde USP in 076mg and 8mg quantities, respectively. The solution must be mixed with Sodium Hydroxide and/or Hydrochloric Acid. It should not be used in series connections, and the unused portion should be discarded. The dosage should be checked before use, and the overwrap should not be removed until ready for use. The overwrap is a moisture barrier; therefore, it must be visually inspected for tears or holes before use. If the overwrap is damaged, discard the unit. Visual inspection is also required post-removal of the overwrap to check for minute leaks. If any leaks are found, discard the solution because it may be ineffective. The product is temperature-sensitive and must be kept within 20-25°C (68-77°F) with excursions permitted from 16-30°C (59-86°F). The product is available in 300mL containers with NDC 0409-4883-11 and the code B wR1532.*

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