Linezolid Injection, Solution
Product Images NDC 63323-713
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Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Linezolid (NDC 63323-713). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fresenius Kabi Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure (Lin0a 0001 02)
Fresenius Kabi Logo (Lin0a 0001 03)
Bag (Lin0a 0001 04)
This is a description of an intravenous injection solution called Linezolid. The solution contains 600mg of Linezolid per 300mL (2mg per mL) and is intended for single-use only. The solution contains linezolid, dextrose, sodium citrate, citric acid, and water for injection. The normal dose for adults is described in the package insert. The solution should not be used in series connections and should be checked for leakage. The solution should be stored between 20°C to 25°C (68°F to 77°F) and should not be frozen. The description also provides information about the manufacturer, including the lot number and expiration date.*
Foilfront (Lin0a 0001 05)
This is a description for Linezolid Injection, indicated for intravenous infusion use only for adults. It is used immediately once removed from the overwrap that serves as a moisture barrier and stored at a controlled room temperature not exceeding 25°C. It is not advisable to use in series connections and to add supplementary medication to avoid sterility impairment. The container closure does not contain natural rubber latex and is manufactured in Norway. However, the dosage and exact indications are found in the package insert.*
Backfoil (Lin0a 0001 06)
Shipper (Lin0a 0001 07)
Product No. 713013 is an injectable solution manufactured by Fresenius under the name Linezolid. Each 300 mL bottle contains 600 mg of the active ingredient (2 mg per mL). The product should be stored at a temperature between 20 to 25°C and should not be frozen. It is sensitive to light. The product is labeled with the NDC code of 63323-713-13 and has an expiration date (MM-DD-YYYY) and lot number. The product is for prescription use only and was made in Norway.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.